Recall
Active
FDA
Official source
Product may be contaminated with Salmonella. Product details: 1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules (120 count) 2. Doctor s Pride Complete Green Superfood...
- Company
- Total Nutrition Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for Salmonella Product details: Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb box
- Company
- International Food Products Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may be contaminated with Salmonella Product details: Al Yaman Halawa Extra Pistachio 907g (31.994 oz) plastic jars, UPC 5 287000 098083, 12 retail units per case
- Company
- GREENWORLD FOOD EXPRESS (USA) LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product tested positive for Salmonella Product details: Legacy Tex Dressing Stabilizer Blend #7604-50, 50lb bags
- Company
- International Food Products Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products were made with recalled California Dairies milk powder due to Salmonella. Product details: White Cheddar Seasoning packed in the following sizes and configurations: 1. Net Wt. 1.2...
- Company
- Jonco Industries
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for Salmonella Product details: Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, 50 lb bags
- Company
- International Food Products Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified...
- Company
- Becton Dickinson & Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified...
- Company
- Becton Dickinson & Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified...
- Company
- Becton Dickinson & Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential Salmonella Javiana contamination Product details: Sirna & Sons Produce PEPPER JALAPENO BREAK 1LB, repackaged into 1 lb. plastic bags, Product Number: 55255, Packed by Sirna &...
- Company
- Sirna and Sons Produce, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may be contaminated with Salmonella. Product details: bettergoods brand Pistachio Nut Butter, NET WT 6.7oz (190g), UPC 194346207961
- Company
- Botticelli Foods, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella. Product details: Whole Foods Medium Pico de Gallo Guacamole Dip, Keep Refrigerated. Packed...
- Company
- WFM Purchasing, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella. Product details: Whole Foods Spicy Guacamole Dip, Keep Refrigerated. Packed in various sized...
- Company
- WFM Purchasing, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40 Product details: Bombay Kitchen brand Tikka Sev; Net Wt 9oz (255g); INGREDIENTS: Chickpea Flour, Water, Non-GMO...
- Company
- Ethnic Foods Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Possible Salmonella in Moringa Leaf Powder product. Product details: Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle....
- Company
- FACTORY6, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may be contaminated with Salmonella Typhimurium Product details: MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER...
- Company
- MOGO Moringa LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with Salmonella Product details: Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER; NET WEIGHT: 15 KGS; packaged in brown paper bags with a white label
- Company
- Trafa Pharmaceutical Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Fillet sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential...
- Company
- Fresh & Ready Foods LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the...
- Company
- Fresh & Ready Foods LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Moringa Powder ingredient positive for salmonella Product details: Organic Moringa Powder; 15kg/bag (bulk); Product code: GJ96
- Company
- Green Jeeva LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Contaminated with Salmonella Product details: 1. TNVitamins 100% Organic Moringa Capsules 1,200 mg 2. TNVitamins 100% Organic Moringa Powder 96 grams
- Company
- Total Nutrition Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination Product details: Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag...
- Company
- The Coffee Connexion Co., Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement. Product details: Zarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon bucket/pail...
- Company
- Zarlengo Italian Ice
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement. Product details: Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6...
- Company
- Zarlengo Italian Ice
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement. Product details: Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16...
- Company
- Zarlengo Italian Ice
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Soba sauce packet, which contains bonito, sardine, and mackerel (fish), was packed into Sura Tanmen Hot and Sour Flavor ramen noodle package kit, but fish species are not declared on...
- Company
- H & U Inc. dba Sun Noodle
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared peanuts. Product details: Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000053
- Company
- KHONG GUAN (HQ)
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Label does not declare walnuts in English Product details: Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc....
- Company
- Byron White Formulas, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object: products may contain glass pieces Product details: Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual fruit...
- Company
- Dreyer's Grand Ice Cream Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object: products may contain glass pieces Product details: Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper outer cartons; individual fruit...
- Company
- Dreyer's Grand Ice Cream Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The product contains 1,4-DMAA, Phenylethylamine and Phenibut. Product details: Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
- Company
- ZMB Enterprises
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product had a presumptive positive test result for Listeria monocytogenes Product details: Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons & White Cheddar Cheese,...
- Company
- CUISINE, KETTLE
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list Product details: Clear glass bottle with black screw lid...
- Company
- Africando Foods LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object: products may contain glass pieces Product details: Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual...
- Company
- Dreyer's Grand Ice Cream Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coconut)....
- Company
- Lidl US TRADING
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object: products may contain glass pieces Product details: Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 ounce, with UPC 041548000121, packaged in paper outer cartons; individual...
- Company
- Dreyer's Grand Ice Cream Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coconut)....
- Company
- Lidl US TRADING
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object: products may contain glass pieces Product details: Outshine Fruit Bars Strawberry, Pineapple, Grape, Tangerine. 24-Count 2.5 ounce, UPC 041548816678, packaged in paper...
- Company
- Dreyer's Grand Ice Cream Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared peanuts. Product details: BLACK AND WHITE GLUTINOUS RICE BALLS WITH BLACK SESAME FILLING NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000084
- Company
- KHONG GUAN (HQ)
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Egg Allergen Product details: Jalapeno Ranch, packed in 16 oz. glass jars, 6 jars per case, with UPC #199284564923.
- Company
- Jaime's Foods ATX, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Label does not declare walnuts in English Product details: Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315...
- Company
- Byron White Formulas, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object: products may contain glass pieces Product details: Outshine Fruit Bars Tangerine, 6-Count 2.5 ounce, with UPC 041548612041, packaged in paper outer cartons; individual...
- Company
- Dreyer's Grand Ice Cream Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Label does not declare walnuts in English Product details: Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas...
- Company
- Byron White Formulas, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may have been improperly pasteurized. Product details: Mehadrin Chocolate Leben; 6 OZ (170g) CUPS, UPC: 070784023144
- Company
- UPSTATE NIAGARA COOPERATIVE
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Inaccurately declared nutrients including Potassium (overstated) and Calcium (overstated). Product details: Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz
- Company
- Prospector Popcorn, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Due to potential E. coli O145:H28 contamination Product details: Organic Whole Mixed Berries, Net Wt. 48 oz (3Lb) plastic bag. packed in 6 bags per case of 10 oz each. Keep Frozen. UPC...
- Company
- Publix Super Markets, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 200 mcg (0.2 mg), packaged in a) 90-count bottles (NDC 16729-457-15) and b) 1000-count bottles (NDC 16729-457-17), Rx...
- Company
- ACCORD HEALTHCARE, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU). Product details: Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules...
- Company
- Hikma Pharmaceuticals USA INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured...
- Company
- ACCORD HEALTHCARE, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617,...
- Company
- ACCORD HEALTHCARE, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617,...
- Company
- ACCORD HEALTHCARE, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 137 mcg (0.137 mg), packaged in a) 90-count bottles (NDC 16729-454-15) b) 1000-count bottles (NDC 16729-454-17), Rx Only,...
- Company
- ACCORD HEALTHCARE, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed content uniformity specifications. Product details: Clobetasol Propionate Cream USP, 0.05%, 60 g tube, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108,...
- Company
- Lupin Pharmaceuticals Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 300 mcg (0.3 mg), 90-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured...
- Company
- ACCORD HEALTHCARE, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617,...
- Company
- ACCORD HEALTHCARE, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of particulate matter: glass and stopper piece Product details: Acthar Gel (repository corticotropin injection), 5 mL multiple-dose vial, Rx Only, Mfd. for: Mallinckrodt ARD LLC,...
- Company
- Mallinckrodt Hospital Products Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617,...
- Company
- ACCORD HEALTHCARE, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing Product details: Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling...
- Company
- Church & Dwight Co., Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), packaged in a) 90-count bottles (NDC 16729-456-15), and b) 1000-count bottles (NDC 16729-456-17), Rx...
- Company
- ACCORD HEALTHCARE, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles. Product details: Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20...
- Company
- Fresenius Kabi USA, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate matter. Product details: Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC...
- Company
- B BRAUN MEDICAL INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain a potentially contaminated component which were recalled by the manufacturer Product details: Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y;...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain a potentially contaminated component which were recalled by the manufacturer Product details: Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF, Medline Kit SKU...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain a potentially contaminated component which were recalled by the manufacturer Product details: Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may...
- Company
- IMRIS Imaging Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may...
- Company
- IMRIS Imaging Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain a potentially contaminated component which were recalled by the manufacturer Product details: Medline convenience kits labeled as: 1) C-SECTION, Medline Kit SKU DYNJ904612L;...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device. Product details: POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider,...
- Company
- Olympus Corporation of the Americas
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar Hemodialysis machines....
- Company
- Fresenius Medical Care Renal Therapies Group, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Software issue may cause measurements to be displayed inaccurately. Product details: Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation
- Company
- Merge Healthcare, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose. Product details: Alphenix Models INFX-8000C...
- Company
- Canon Medical System, USA, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. Product details: Halyard TOTAL JOINT Model/Catalog Number:...
- Company
- AVID Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain a potentially contaminated component which were recalled by the manufacturer Product details: Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine. Product details: Kian Pee Wan Capsules, 30-count bottles
- Company
- Buy-Herbal
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations:Noted during FDA inspection Product details: SILDENAFIL CITRATE USP, 0.100 KG, 100 gm-bag Net Wt, RX ONLY "FOR Prescription Compounding Only", Shoolin Pharma Chem LLP,...
- Company
- Shoolin Pharma Chem LLP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material Product details: SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile...
- Company
- Apollo Care, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin. Product details: Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL...
- Company
- Victory Medical Center Pharmacy
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material Product details: SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only,...
- Company
- Apollo Care, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material Product details: SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx...
- Company
- Apollo Care, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass. Product details: Optiray Imaging Bulk Package-350, Ioversol Injection 74%,...
- Company
- Liebel-Flarsheim Company LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles. Product details: CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION, USP, 75 mg/5 mL,...
- Company
- Heritage Pharmaceuticals Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material Product details: SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile...
- Company
- Apollo Care, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material Product details: SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx...
- Company
- Apollo Care, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material Product details: SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only,...
- Company
- Apollo Care, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of assurance of sterility. The recall is due to potential contamination Product details: CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by...
- Company
- Prestige Brands Holdings
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material Product details: SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile...
- Company
- Apollo Care, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material Product details: SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile...
- Company
- Apollo Care, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter Product details: Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL) Single-Dose Infusion Bag in 100mL GALAXY Plastic Container, Frozen Premix,...
- Company
- Baxter Healthcare Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010). Product...
- Company
- W L Gore & Associates, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. Product details: Cardinal Health Presource Kits: 1) ENT...
- Company
- Cardinal Health 200, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if...
- Company
- Covidien, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to an increase rate of balloon pinhole defects. Product details: BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in...
- Company
- MICROVENTION INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. Product details: Cardinal Health Presource Kits: 1)...
- Company
- Cardinal Health 200, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life. Reduced...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. Product details: Cardinal Health Presource Kits: 1) KIT,...
- Company
- Cardinal Health 200, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Firmware issue potentially leading to loss of geometry movements. Product details: Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058....
- Company
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire. Product details: GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The...
- Company
- Terumo Medical Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life. Reduced...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Manufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance. If the product sterility is compromised, patients may be exposed to microorganisms,...
- Company
- Spectra Medical Devices, Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position. Product details:...
- Company
- Baxter Healthcare Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits. Product details: Boston Scientific Enhance...
- Company
- Galt Medical Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if...
- Company
- Covidien, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products may be contaminated with Listeria monocytogenes. Product details: Selectos Latinos Requeson Mexicano Mexican Cottage Cheese, Net Weight 16 oz, packed into retail-sized clear...
- Company
- La Colonia Foods Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, mild cheese variety (Snack Pack Assorted Regular Mild Stix White Colby, Marble Jack, Yummy...
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Soy. The firm received complaints of sausage in the burritos. Upon review the firm discovered the sausage contains soy which is not listed on the label. Product details: Spicy...
- Company
- M.G. Foods, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Pepper Jack Cheese Varieties (Jalapeno Cheddar, Pepper Jack, Sizzlin Colby with Habanero Peppers)....
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Mild Cheese Variety (Yummy Cheddar, White Cheddar, White Colby, Monterey Jack, Marble Jack). Sold...
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Pepper Jack Cheese Varieties (Snack Pack Assorted Pepperjack Stix (Jalapeno Cheddar, Pepper...
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Possible foreign object (thin, soft plastic strands). Product details: Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree, 4oz/113g pouch, UPC 815367010780, PTO Item 10720....
- Company
- PT Organics Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Soft Cuajada in Brine, sold in five (5) gallon and two (2) gallon buckets. Unknown information:...
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Sharp Cheese Snack Pack Sharp Stix White or Yellow. Sold in approximate 0.40-lb (6.4oz) units....
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Pepper Jack Cheese Varieties (3-in-a-Pack Assorted Jalapeno Cheddar, Pepper Jack, Sizzling Colby)....
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Soft Ricotta (Requeson), and Soft Ricotta with Jalapenos (Requeson Con Chile). Sold in 2- and...
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, mild cheese variety (Fresh Cheddar Curd). Sold in approximate 0.75-lb and 1.5-lb box units....
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Flexible food pouch may release thin plastic strips into food. Product details: Flexible food pouch (3-layer foil, spouted, #CP6088), manufactured for packaging Pumpkin Tree Peter Rabbit...
- Company
- CHEER PACK
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Flavored Cheese (Old Bay Cheddar). Sold in approximate 1/2-lb, 1-lb, 2.5-lb, 5-lb, and 40-lb...
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared tadalafil Product details: Ashfiat Alharamain Energy Support 250ml/8fl. oz.
- Company
- AKKARCO LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared milk from lactose. Product details: Big Way Hot Pot "Hot Pot Miso Paste"; 1kg (35.3oz) unit package. Product is packaged in generic bulk packaging.
- Company
- Big Way Ca Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign Manufacturer label contains Undeclared allergen ingredients Wheat, Soy, Sesame, Yellow #5 and Blue #1 in Frozen Flounder Products. Product details: FLOUNDER SASHIMI WITH SAUCE;...
- Company
- Eunha Fisheries Co., LTD
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Possible Salmonella Enteritidis Product details: Grade A White In-shell Chicken eggs packaged in the following configurations: 1. Kroger, Medium, 12 Eggs, Net Wt 21 oz (1lb 5oz) 596g, UPC...
- Company
- MIDWEST POULTRY SERVC C/O H & LELECTRIC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared peanuts Product details: Dark Chocolate Coconut Almond Bites, 3.17oz, Plastic Pouches, 10 Packages per case.
- Company
- Bazzini LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential Cyclospora contamination. Product details: MARKON BLEND LETT/ROM 80/20 WITH SEP BAGGIES 4/5# Iceberg, Romaine, Carrots, Red Cabbage products.
- Company
- Taylor Farms de Mexico S. de R.L. de C.V.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Red #40. Product details: Honeyville YELLOW COLOR 1 GALLON NFI: WATER, FD&C YELLOW #5, FD&C YELLOW #6, CITRIC ACID, AND SODIUM BENZOATE. MANUFACTURED FOR: HONEYVILLE, INC....
- Company
- FlavorsandColor.Com
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Label declares cream and cheese, but Milk is not declared Product details: Vodka Tomato Sauce, NET WT. 24 oz / 680g, glass jar packed 12 jars in a carton.
- Company
- SHEANDRO LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Possible Salmonella Enteritidis Product details: Grade A Brown In-shell Chicken eggs packaged in the following configurations: 1. Simple Truth, Natural Cage Free Grain Fed, Medium, 12...
- Company
- MIDWEST POULTRY SERVC C/O H & LELECTRIC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared allergen (egg) Product details: KC Everyday Mac & Cheese, 3lb x 6. Item # 20609055. 6 - 3 lb pouches, Net Wt: 18 lb. (8.16Kg). Fully Cooked. Keep Frozen. Distributed By: Kerry...
- Company
- Kerry, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility Product details: Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 90, 0.2%), Sterile 0.4 FL OZ (13 mL), Distributed by: The...
- Company
- Rohto-Mentholatum (Vietnam) Co., Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR...
- Company
- Major Pharmaceuticals
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility Product details: Rohto Cooling Eye Drops Cool Relief (naphazoline hydrochloride 0.012%, polysorbate 80 0.2%), Sterile, 0.4 FL OZ (13 mL) each, Distributed...
- Company
- Rohto-Mentholatum (Vietnam) Co., Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR...
- Company
- Major Pharmaceuticals
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations: Product quality complaints concerning abnormal texture or consistency (described as grainy, gritty, or sandy) were received. Product details: Azelaic Acid Gel, 15%, 50...
- Company
- Glenmark Pharmaceuticals Inc., USA
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of precipitate Product details: Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per carton, Rx only, Manufactured for: Mylan Institutional LLC,...
- Company
- MYLAN PHARMACEUTICALS INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops. Product details: Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0.5%,...
- Company
- MICRO LABS USA INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Incorrect Product Formulation Product details: Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Compound Volume 416.8 mL per bag, Rx only, Single Dose...
- Company
- Central Admixture Pharmacy Services Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
undeclared egg Product details: Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES, 4.5 oz clear plastic package
- Company
- Blank Slate Creamery Production
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Smoked Pepper Cheese Varieties (Jalapeno Cheddar), sold in 1/2-lb and 1-lb units. Unknown...
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign Manufacturer label contains Undeclared allergen ingredients Wheat, Soy, Sesame, Yellow #5 and Blue #1 in Frozen Flounder Products. Product details: Sliced Korean Halibut with Soy...
- Company
- Eunha Fisheries Co., LTD
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Soft Cuajada crumbs. Unknown information: packaging, labeling, or total quantity of product...
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Allergen missing from contains statement: fish Product details: "***Hondashi 0.25oz***" seasoning packed in silver plastic/metallic pouch, pouches packed in brown paperboard cartons (600...
- Company
- Pack'n Fresh LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Soft Cuajada (vacuum sealed), sold in 14oz- and 2.5 lb clam shells, and 5-lb bags. Unknown...
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contaminated with Listeria monocytogenes. Product details: Clover Hill Dairy LLP, Smoked Cheddar Cheese Varieties (Cheddar, White Cheddar). Sold in 1/2-lb and 1-lb units. Unknown...
- Company
- Clover Hill Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
shortfill; reports of empty capsules. Product details: Dicyclomine Hydrochloride Capsules, USP, 10mg, 1,000 bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279...
- Company
- Aurobindo Pharma USA Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter; identified as stainless steel Product details: Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove...
- Company
- Sunny Pharmtech Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP: Due to Out of Specification (OOS) result for N-Nitroso Mirabegron impurity. Product details: Mirabegron Extended-Release Tablets, 25 mg, 30-count bottle, Rx only, Manufactured by:...
- Company
- Zydus Pharmaceuticals (USA) Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter; identified as stainless steel Product details: Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove...
- Company
- Sunny Pharmtech Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability Product...
- Company
- Ascend Laboratories, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability Product...
- Company
- Ascend Laboratories, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability Product...
- Company
- Ascend Laboratories, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2. While the assay results were not impacted, the overall health...
- Company
- Siemens Healthcare Diagnostics, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. Product details: Brand Name: U2 Total Knee System Product Name:...
- Company
- United Orthopedic Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely depressed Atellica CH Enzymatic...
- Company
- Siemens Healthcare Diagnostics, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to a defective circuit board that overheats Product details: Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software Version:...
- Company
- Oxos Medical Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Devices could potentially contain an occluded or partially occluded Guedel Airway tip. Product details: FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12). REF Number: 1011-40002....
- Company
- INTEGRATED MEDCRAFT LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Software issue issue with the MAC VU360 v3.0 system. After selecting the order refresh icon, an open preview or review screen might fail to close automatically after 2 minutes of...
- Company
- GE Medical Systems Information Technologies Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications." Product details: REF # D23354,...
- Company
- Beckman Coulter Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large Esophageal and Tracheal Flange...
- Company
- Freudenberg Medical, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant. Product details: Brand Name: U2 Total Knee System...
- Company
- United Orthopedic Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds....
- Company
- AVID Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for breach in sterile barrier of device packaging. Product details: Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN: Radial Jaw 4 Jumbo 240cm Box 5;...
- Company
- Boston Scientific Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. Product details: Brand Name: U2 Total Knee System Product Name:...
- Company
- United Orthopedic Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the...
- Company
- Pride Mobility Products Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the...
- Company
- Pride Mobility Products Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Nuez, 1 Bar (81.7 g), with UPC 827912008548
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Tamarindo, 1 Bar (81.7 g), with UPC 827912008593
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than...
- Company
- Nutricia North America
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Arroz con Leche, 4 oz (85 g), with UPC 710594511843
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared peanuts Product details: OLA-OLA POUNDED GROUNDNUTS (INTWILO) NET WT. 32 oz., 2 lbs. (0.907 kg) Distributed by: Yusol International Foods Sacramento, CA 95828 Product of USA...
- Company
- Fayus Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign material (Glass) was found in the product. Product details: Ruby, Artichoke Hearts Quartered, 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G), Can, 6 cans per case, Store in dry...
- Company
- GELLERT GLOBAL GROUP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Fresa Leche, 4 oz (85 g), with UPC 710594511850
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Mango, 3.7 oz (81.7 g), with UPC 827912008494
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Limon, 4 oz (85 g), with UPC 710594511836
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Cookies Cream, 1 Bar (81.7 g), with UPC 710594511362
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Pistachio, 1 Bar (81.7 g), with UPC 827912008487
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Ambient storage of the product may lead to Clostridium botulinum toxin formation. Product details: Brooklyn Roasting Company Pasteurized Cold Brew Concentrate; 2.5gal; bag in a box...
- Company
- Brooklyn Roasting Works LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors: Yellow#5, and Yellow#6. Product details: Man Fon Inc. Won Ton Wrappers Extra Thin; Net Wt. 10 oz; UPC# 757168 977315, Keep Refrigerated, Can be Frozen. Sold in 48 units...
- Company
- Man Fon, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
No labeling. Undeclared wheat and colors: Yellow#5, Yellow#6. Product details: Wonton Wrappers packed into clear flexible plastic bag and sold as 40 units (16oz bags)/case. Wonton Wrappers...
- Company
- Man Fon, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Unapproved food additive: sassafras bark. Product details: Vintage Roots Root Beer Syrup, packaged in glass bottle. Net Wt. 8oz. (236.6 mL). Distributed by Vintage Roots, PO Box 12, Brady,...
- Company
- Vintage Roots LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam. Product details: Modern Warrior Ready, Dietary Supplement, 60 CAPSULES
- Company
- Modern Warrior Life, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared sodium tripolyphosphate (STTP) Product details: Island Pacific IMITATION CRAB FLAKES NET WT: 1.0 LB (454g) UPC: 0000000175012 PRECOOKED SERVE HOT OR COLD INGREDIENTS: POLLOCK...
- Company
- Shandong Ling Xian Food Co.,LTD
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared sodium tripolyphosphate (STTP) Product details: Island Pacific IMITATION CRAB STICKS NET WT: 1.0 LB (454g) UPC: 0000000175029 PRECOOKED SERVE HOT OR COLD INGREDIENTS: POLLOCK...
- Company
- Shandong Ling Xian Food Co.,LTD
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared sodium tripolyphosphate (STTP) Product details: NAUTILUS IMITATION CRAB STICKS NET WT: 1.0 LB (454.0g) UPC: 878665000235 Precooked - serve hot or cold Ingredients: Pollock...
- Company
- Shandong Ling Xian Food Co.,LTD
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Allergen (Fish) Product details: Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wrapper, 12 packages per case , 6 ea: Kimchi & Tofu Kimbap / 6 ea...
- Company
- GELLERT GLOBAL GROUP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR...
- Company
- Major Pharmaceuticals
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter: Hair was found in products Product details: Naropin (ropivacaine hydrochloride Injection, USP), 0.5%, 100 mg per 20 mL (5 mg per mL), Twenty-five, 20 mL...
- Company
- Fresenius Kabi USA, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR...
- Company
- Major Pharmaceuticals
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 125 mcg (0.0125 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR...
- Company
- Major Pharmaceuticals
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR...
- Company
- Major Pharmaceuticals
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility Product details: Rohto Cooling Eye Drops Digi Eye (hypromellose 0.35%, tetrahydrozoline HCl 0.05%), Sterile, 0.4 FL OZ (13 mL), Distributed by: The...
- Company
- Rohto-Mentholatum (Vietnam) Co., Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter: Hair was found in products Product details: Xylocaine (lidocaine HCl Injection, USP), 1%, 200 mg per 20 mL (10 mg per mL), 25 Multiple-Dose Vials, 20 mL, Rx...
- Company
- Fresenius Kabi USA, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Foreign material found in product (identified as metal shavings) Product details: DQ Chocolate Reduced Fat Ice Cream Mix, 5 GAL (18.9L). Keep refrigerated.
- Company
- Galliker Dairy Co, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products may be contaminated with Listeria monocytogenes. Product details: Requeson (soft ricotta) 1 lb. packed into a clear clamshell package with no labeling information. "Requeson" is...
- Company
- Nelson & Isa Lacteos LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Firm's finished product label does not declare the source of marine collagen which was determined to be fish. Product details: Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2...
- Company
- Mellish Island Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed impurity/degradation specification:12M Long-term Stability conditions (25 ¿2 ¿C/60 ¿5%RH), an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III...
- Company
- Ascend Laboratories, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris...
- Company
- Windstone Medical Packaging, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID. Product details: Brand Name:...
- Company
- Instrumentation Laboratory
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. Product details: Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number:...
- Company
- Stryker GmbH
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation,...
- Company
- Medtronic Perfusion Systems
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. Product details: Stryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number:...
- Company
- Stryker GmbH
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of ventilation therapy. Product...
- Company
- ResMed Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were filled with approx. 4.5 cc DBM...
- Company
- IsoTis OrthoBiologics, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. Product details: Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number:...
- Company
- Stryker GmbH
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential E. coli O145:H28 Contamination Product details: Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 10 oz each. Keep Frozen
- Company
- Frutas y Hortalizas del Sur S.A.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Pina Colada, 1 Bar (81.7 g), with UPC 710594511225
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than...
- Company
- Nutricia North America
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility Product details: Rohto Cooling Eye Drops Dry Aid (povidone 0.68%, propylene glycol 0.3%), Sterile, 0.34 FL OZ (10 mL), Distributed by: The Mentholatum...
- Company
- Rohto-Mentholatum (Vietnam) Co., Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 50 mcg (0.050 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR...
- Company
- Major Pharmaceuticals
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter: Hair was found in products Product details: Lidocaine HCl Injection, USP, 2%, 100 mg per 5 mL (20 mg per mL), 25 Single Dose Vials, 5 mL per vial, Rx only,...
- Company
- Fresenius Kabi USA, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orientation...
- Company
- Boston Scientific Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for use with the FARAPOINT PFA catheter. Product details: FARASTAR...
- Company
- Boston Scientific Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage. Product details: Halyard...
- Company
- AVID Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to manufacturing issues, reperfusion catheters may fractures Product details: Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
- Company
- Penumbra, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as system...
- Company
- Alphatec Spine, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the associated alerts will not be triggered...
- Company
- Medtronic MiniMed, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to quality issues that could...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent application at the tubing to return...
- Company
- ICU Medical Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for gynecology use, which could impact...
- Company
- Karl Storz Endoscopy
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information. Product details: FARASTAR Pulsed Field Ablation Generator,...
- Company
- Boston Scientific Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case condition, rail mechanism may become...
- Company
- Ferno-Washington Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species. Product details:...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Impurities/Degradation Specifications Product details: Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured by: OneSource Specialty, Pharma...
- Company
- ONESOURCE SPECIALTY PHARMA LIMITED
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator Product details: BD ChloraPrep Clear, (2% w/v chlorhexidine...
- Company
- CareFusion 213, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility Product details: CLEVIPREX (clevidipine injectable emulsion) 50 mg/100 mL (0.5 mg/mL), 10 Single Use Vials, Rx Only, Manufactured for: Chiesi USA, Inc.,...
- Company
- Chiesi USA, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Product details: QC Quality Choice, Carbamide Peroxide, 6.5%, 0.5 FL. OZ. (15 mL) a) Washer Bulb included...
- Company
- Bell Pharmaceuticals, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Product details: Clinere, Carbamide Peroxide, a) 2 bottles of Clinere Carbamide Peroxide (2 x 0.50 mL)...
- Company
- Bell Pharmaceuticals, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Product details: LEADER, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit -1 RUBBER BULB SYRINGE, 0.5 FL...
- Company
- Bell Pharmaceuticals, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Product details: FAMILY Wellness, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), Kit - Washer Bulb Included,...
- Company
- Bell Pharmaceuticals, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Product details: CAREone, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Bottle, NDC 72476-838-34,...
- Company
- Bell Pharmaceuticals, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug: Low out of specification assay results performed during long-term stability testing. Product details: Nystatin Cream USP, (100,000 USP Nystatin Units), NET WT 15 g, Rx...
- Company
- Padagis US LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Product details: meijer, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Washer Bulb included, NDC...
- Company
- Bell Pharmaceuticals, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Product details: CVS Health, Carbamide Peroxide, 6.5%, 0.5 FL Oz (15 mL), a) Bottle (NDC 51316-822-00.);...
- Company
- Bell Pharmaceuticals, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Product details: TopCare Health, CARBAMIDE PEROXIDE 6.5%, 0.5 FL OZ (15 mL) a) Kit - WASHER BULB & DROPS...
- Company
- Bell Pharmaceuticals, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Product details: AUDIOLOGIST'S CHOICE, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL) a) Kit - Washer Bulb...
- Company
- Bell Pharmaceuticals, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Product details: GOOD NEIGHBOR PHARMACY, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit - Washer Bulb...
- Company
- Bell Pharmaceuticals, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Product details: Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01,...
- Company
- Bell Pharmaceuticals, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111 Product...
- Company
- Orthofix U.S. LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the manifold, resulting in loose...
- Company
- Boston Scientific Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually...
- Company
- Abiomed, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for brush heads to break. Product details: Papablic Replacement Brush Heads. Model Number: PAPA317AA.
- Company
- Papablic Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for brush heads to break. Product details: Papablic Replacement Brush Heads. Model Number: Papablic18B
- Company
- Papablic Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually...
- Company
- Abiomed, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at the programmed rate. Product...
- Company
- ICU Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000 instead of ~5000). Product...
- Company
- Daavlin Distributing Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been...
- Company
- GE Medical Systems, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually...
- Company
- Abiomed, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices. Product...
- Company
- Olympus Corporation of the Americas
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region....
- Company
- Oscor Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000 instead of ~5000). Product...
- Company
- Daavlin Distributing Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been...
- Company
- GE Medical Systems, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. Product details: General Biospy...
- Company
- Argon Medical Devices, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Nanche, 1 Bar (81.7 g), with UPC 827912008449
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for spoilage. Product details: Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl. Cover. Cook for 1.5-2 minutes....
- Company
- AMY'S KITCHEN INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Mamey, 1 Bar (81.7 g), with UPC 827912008456
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Grocella, 1 Bar (81.7 g), with UPC 827912008531
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Vainilla, 4 oz (85 g), with UPC 710594511829
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may contain metal fragments. Product details: WY Duck Sauce, 0.35 oz. (10 g), flexible film packets, 500 packets per case.
- Company
- W.Y. Industries, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Coconut, 4 oz (85 g), with UPC 710594511867
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Undeclared milk allergen. Product details: Winfield's CWB Chocolate Bar, packed in clear cello bag with fabric bow on top. Manufactured by CBSL Commissary (DBA Winfield's Chocolate Bar)...
- Company
- Chocolate Bar Holdings LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Product details: Ice Pop, D'Dioses Rompope, 4 oz (85 g), with UPC 710594511812
- Company
- D'Dioses Fruit Pops, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential foreign material (glass) Product details: Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48kg) Package UPC 721582-13283 4. Case UPC...
- Company
- General Mills James Ford Bell Technical Center
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential foreign material (glass) Product details: Pillsbury Bread Rolls, Kaiser Roll Dough. 144 units / 2.5oz each. Net Wt. 22.5 lb (10.2kg) Package UPC 7 21582-13288 9. Case UPC...
- Company
- General Mills James Ford Bell Technical Center
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product not adequately pasteurized Product details: Joy Pineapple Lassi 16 oz.
- Company
- Joy Gourmet Foods LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Improperly eviscerated which may result in Clostridium botulinum contamination Product details: Dried Herring Fish 7 oz.
- Company
- Prime Food Processing LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with plastic material Product details: MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 oz. (298g), packaged in a resealable...
- Company
- MARS SNACKING
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Undeclared allergen (milk) and process deviation (product not held under refrigeration as required) Product details: Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear...
- Company
- Fry Pie Factory LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared peanuts. Product details: FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. (255g) UPC 797565011830 INGREDIENTS: DARK CHOCOLATE (SUGAR, CHOCOLATE LIQUOR, COCOA BUTTER, MILK FAT,...
- Company
- Western Mixers Produce & Nuts, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Dietary supplement product Vista MAX contains undeclared Yellow#5. Product details: Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health,...
- Company
- Provision Health Corp. dba PH Labs
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Dietary supplement product Ocular Plus contains undeclared Yellow#5. Product details: Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Serving Size:...
- Company
- Provision Health Corp. dba PH Labs
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Elevated coliforms Product details: Plastic 1-gallon clear pail blue label which reads in part as "BLUE RIBBON CLASSICS FRENCH VANILLA, MFD. BY WELLS ENTERPRISES, INC. D/B/A WELLS DAIRY,...
- Company
- Wells Enterprises, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may be contaminated with Clostridium botulinum. Product details: a.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0-12 months; NET WT 24.7...
- Company
- NARA ORGANICS INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with plastic material Product details: MorningStar Farms Hot & Spicy Sausage Patties, 100% Plant Protein Vegan Sausage Patties, Net Wt. 8 oz. (228g), packaged in a...
- Company
- MARS SNACKING
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Sesame allergen Product details: Smoked Sausage Spice 32.86#
- Company
- Adams Extract & Spice LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
undeclared soy Product details: Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough, 8-oz pouch 12 cookies per pouch, UPC 8 50073 08700 8, 8 pouches per case
- Company
- Bear Stewart Co
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Sesame allergen Product details: EC Hot Links Seasoning 45.05#
- Company
- Adams Extract & Spice LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3. Product details: Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case,
- Company
- Wise Foods Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Allergen (Soy) Product details: Vanilla Dessert Shells (Giant), 6 dessert shells/1 package, 1 dessert shell is approximately 23.67 grams. 1package is 142 grams. 1 package has 1...
- Company
- Specialty Bakers, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Sesame allergen Product details: Coopers Bbq 60 Gal Bean Mix box
- Company
- Adams Extract & Spice LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign material: small metal pieces Product details: Alabama Banana Pudding Marshmallow, 4 ounce 16 pieces of individual marshmallows packaged in a sealed plastic bag inside a printed...
- Company
- Wondermade LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Sesame allergen Product details: JB Chicken Sknls 35.73#
- Company
- Adams Extract & Spice LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging. Product details: High Valley Orchard Chocolate Covered Raisins,...
- Company
- Lehi Valley Trading Company, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Sesame allergen Product details: Johnny's Salad and Pasta Elegance 5.5 oz (UPC: 0-70381-10014-9) " Johnny's Salad and Pasta Elegance 2.75 oz (UPC: 0-70381-10013-2)
- Company
- Adams Extract & Spice LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
undeclared colors (yellow#5) Product details: Le Chef Bakery branded Mini Italian Pastry Assortment; 2.5 lbs/cs; (40 pieces/cs); packaged in generic food service packaging with white...
- Company
- Le Chef Bakery
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent drug Product details: Gasco Isopropyl Alcohol 70%, Net Contents: 1 US Gallon (3.78 L), Manufactured by: Gasco Industrial Corp., PO Box 1360, Gurabo, PR 00778, Made in USA
- Company
- Gasco Industrial Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent drug Product details: Gasco Isopropyl Alcohol 70%, 32 oz (946 mL) Gasco Industrial Corp., PO Box 1360, Gurabo PR 00778, UPC 7 87302 12363 6.
- Company
- Gasco Industrial Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent drug Product details: Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 32 oz., 946 mL, Distributed by: Drogueria San Juan, Calle De Diego 590, Sabana Llana Rio Piedras, PR...
- Company
- Gasco Industrial Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
cGMP deviations Product details: Clomiphene Citrate USP Active Pharmaceutical Ingredient (CAS : 50-41-9), Net Weight a)1 KG (NDC 84849-000-01), b) 500 g (NDC 84849-000-02), (c) 100 g (NDC...
- Company
- Shimoga Chemicals
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Sterility Assurance Product details: Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset...
- Company
- Reliance Life Sciences Private Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent drug Product details: Gasco Isopropyl Alcohol 70%, Net Contents: 16 Oz. (474 mL). Manufactured by: Gasco Industrial Corp., PO Box 1360 Gurabo PR 00778 Made in USA UPC 7 87302...
- Company
- Gasco Industrial Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent drug Product details: Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 1 gallon (3.78 liter), Distributed by: Drogueria San Juan, Calle De Diego 590, Sabana LLana Rio...
- Company
- Gasco Industrial Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Sterility Assurance Product details: Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use, Manufactured for: Somerset Therapeutics,...
- Company
- Reliance Life Sciences Private Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Sterility Assurance Product details: Pemetrexed for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset...
- Company
- Reliance Life Sciences Private Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Sterility Assurance Product details: Azacitidine for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For Subcutaneous and Intravenous Use, Rx only, Manufactured for:...
- Company
- Reliance Life Sciences Private Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification. Product details: Medline Remedy Specialized Silicone Cream (Hydraguard-D ),Manufactured for...
- Company
- BioMed Laboratories, LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent drug Product details: Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 16 oz, 474 mL, Distributed by: Drogueria San Juan, Calle De Diego 590, Sabana LLana Rio Piedras, PR...
- Company
- Gasco Industrial Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Impurities/Degradation Specifications Product details: Methohexital Sodium, 100 mg/10 mL (10 mg/mL), Total Volume: 10 mL, Rx only, Compounded drug, QuVa Pharma, 1075 W Park One Dr,...
- Company
- QuVa Pharma, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry Product details: TERPENICOL Antifungal Solution, (Undecylenic...
- Company
- Blaine Labs Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Surgical dressing manufactured out of specification (greater thickness). Product details: Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
- Company
- ConvaTec, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results. Product details: GSP...
- Company
- WALLAC OY
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
A product error defect may cause incorrect bracket placement. Product details: KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,
- Company
- Klowen Braces
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages...
- Company
- Medtronic MiniMed, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers. Product details: Olympus Single Use...
- Company
- Olympus Corporation of the Americas
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk. Product details: Brand Name: Versius Surgical System US Product Name: Vesius...
- Company
- CMR SURGICAL LIMITED
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely elevated HbA1c patient...
- Company
- Siemens Healthcare Diagnostics, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. Product details: Brand Name: Fletcher CT/MR Shielded...
- Company
- Elekta, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X CAREsystem. Product details: 5008X...
- Company
- Fresenius Medical Care Holdings, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. Product details: Brand Name: Brachytherapy Applicator...
- Company
- Elekta, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. Product details: Brand Name: Geneva Product Name:...
- Company
- Elekta, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array. Product details: TMINI Femur Tracking Array REF 109003 UDI-DI...
- Company
- Think Surgical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures. Product details: VITEK 2 AST-N447...
- Company
- Biomerieux Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached could lead to severe...
- Company
- Boston Scientific Neuromodulation Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential presence of Salmonella. Product details: 1.5oz, 2oz Dirty Brand Salt and Vinegar Potato Chips , Plastic Bag.
- Company
- Utz Quality Foods, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared allergen, sesame. Product details: boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels NET WT 26.5 OZ (1.66 LB) 750g Ingredients: Organic wheat flour ... Contains Wheat...
- Company
- Boichik Bagels, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential presence of Salmonella. Product details: 2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag.
- Company
- Utz Quality Foods, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential presence of Salmonella. Product details: 1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.
- Company
- Utz Quality Foods, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
potential salmonella contamination Product details: Motor City Pizza Co. 5 Cheese Bread Single retail pack; 22.43 oz. (1 lb. 6.4 oz.) 636g UPC 8 70375 00511 1; 6 retail units per case...
- Company
- Champion Foods, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product not adequately pasteurized Product details: Joy Saffron Cardamon Lassi 16 oz.
- Company
- Joy Gourmet Foods LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential Salmonella contamination Product details: Spring & Mulberry Mango Chili Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470033,...
- Company
- Spring & Mulberry Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. Product details: 6/11oz No Salt Sunflower Seeds
- Company
- George J Howe Company, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential Salmonella contamination. Product details: Spring & Mulberry Mulberry Fennel Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a burgundy box, UPC...
- Company
- Spring & Mulberry Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product not adequately pasteurized Product details: Joy Plain Chaash Lassi 16 oz., 64 oz.
- Company
- Joy Gourmet Foods LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product not adequately pasteurized Product details: Joy Rose Lassi 16 oz.
- Company
- Joy Gourmet Foods LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. Product details: 25# Sunflower Seeds C/S
- Company
- George J Howe Company, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Incorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub sandwich Product details: Roast beef and cheddar closed face sandwich...
- Company
- Produce Innovations
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product not adequately pasteurized Product details: Joy Sweet Lassi 16 oz.
- Company
- Joy Gourmet Foods LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the...
- Company
- CareFusion 213, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the...
- Company
- CareFusion 213, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the...
- Company
- CareFusion 213, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). Product details: Cinacalcet Hydrochloride Tablets, 30 mg, 30-count bottle, Rx Only, Manufactured...
- Company
- Cipla USA, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility Product details: Accucaine, Kit contains: Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL single dose ampule, Rx Only, Distributed by Enovachem...
- Company
- Asclemed USA Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Foreign Substance Product details: prednisoLONE Acetate Ophthalmic Suspension, USP, 1%, Rx only, Sterile, a) 5 mL (NDC 70748-332-02); b) 10 mL (NDC 70748-332-03), c) 15 mL...
- Company
- Lupin Pharmaceuticals Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the...
- Company
- CareFusion 213, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Levothyroxine Sodium Tablets, USP, 300 mcg (0.3mg), 90 Tablets bottles, Rx only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured...
- Company
- ACCORD HEALTHCARE, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). Product details: Cinacalcet Hydrochloride Tablets, 90 mg, 30-count bottle, Rx Only, Manufactured...
- Company
- Cipla USA, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). Product details: Cinacalcet Hydrochloride Tablets, 60 mg, 30-count bottle, Rx Only, Manufactured...
- Company
- Cipla USA, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility Product details: Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL single dose ampule, Rx Only, Distributed by Enovachem Pharmaceuticals, Torrance, CA 90501,...
- Company
- Asclemed USA Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of assurance of Sterility: Product details: IMULDOSA, (ustekinumab-srlf) Injection, 130 mg/26 mL (5mg/mL), Rx only, Single dose vial, Manufactured by Accord BioPharma Inc., 8041 Arco...
- Company
- ACCORD BIOPHARMA INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Reduced or no recovery of some strains of Neisseria gonorrhoeae. Product details: GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460
- Company
- Remel, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the...
- Company
- RAYSEARCH LABORATORIES AB
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Product details:...
- Company
- Bard Access Systems, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential sterile breach of the pouches in which devices are packaged. Product details: CRE Pro Wireguided 12-15mm 240cm
- Company
- Boston Scientific Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to out-of-specification, or potential out-of-specification, levels of endotoxins Product details: Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton)...
- Company
- TELEFLEX LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients,...
- Company
- Masimo Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Product details: 5855240...
- Company
- Bard Access Systems, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications. Product details: Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557
- Company
- Carl Zeiss Meditec AG
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary...
- Company
- Insulet Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential presence of Salmonella. Product details: 2.0 oz Dirty Maui Onion Chip, Plastic Bag.
- Company
- Utz Quality Foods, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product not adequately pasteurized Product details: Joy Mango-Pina-Strawberry Lassi 16 oz.
- Company
- Joy Gourmet Foods LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product not adequately pasteurized Product details: Joy Mango-Pina-Orange Lassi 16 oz., 64 oz.
- Company
- Joy Gourmet Foods LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product not adequately pasteurized Product details: Joy Masala Chaash Lassi 16 oz., 64 oz.
- Company
- Joy Gourmet Foods LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential Salmonella contamination Product details: Spring & Mulberry Sea Salt Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a grey box, UPC 850055470071, Dist....
- Company
- Spring & Mulberry Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential Salmonella contamination Product details: Spring & Mulberry Lavender Rose Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light blue box, UPC...
- Company
- Spring & Mulberry Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product not adequately pasteurized Product details: Joy Mango Lassi 16 oz., 64 oz.
- Company
- Joy Gourmet Foods LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential Salmonella contamination Product details: Spring & Mulberry Mixed Berry Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470026,...
- Company
- Spring & Mulberry Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product not adequately pasteurized Product details: Joy Strawberry Lassi 16 oz.
- Company
- Joy Gourmet Foods LLC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg. Product details: Lacosamide Tablets, USP, C V,...
- Company
- Annora Pharma Private Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Foreign Substance. Product details: Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy. NDC 55513-810-60
- Company
- Amgen, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Foreign Substance. Product details: Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC 55513-800-99), and b) 60 tablet bottles (NDC 55513-800-60), Rx...
- Company
- Amgen, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations Product details: Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules, Manufactured by: Ajanta Pharma Limited, India, Marketed by: Ajanta Pharma USA Inc. Bridgewater, NJ...
- Company
- Ajanta Pharma USA Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations Product details: Sensipar (cinacalcet) Tablets, 60mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA 91320-1799, Made in Japan....
- Company
- Amgen, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
sub potency Product details: Povi-One, 10% Povidone-Iodine Oral Antiseptic, Packaged by Elevate Oral Care, LLC, 346 Pike Road, Suite 6, West Palm Beach, FL 33411, NDC 57511-0611-1.
- Company
- Elevate Oral Care
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit Product details: DULOXETINE D/R, a) 30 mg (NDC 61919-482-30), 30 Caps; b) 30 mg (NDC...
- Company
- Direct Rx
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area. Product details: BD ChloraPrep FREPP Clear, (2% w/v chlorhexidine gluconate (CHG) and...
- Company
- CareFusion 213, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Carton Label: MAJOR, Methylergonovine Maleate Tablets, USP, 0.2 mg, 20 TABLETS (2 x 10), Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS,...
- Company
- The Harvard Drug Group LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility Product details: PReye Vitamin See Antioxidant Preservative Free Eye Drops, Distributed by: PReye, LLC, Golden, CO
- Company
- PReye LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance Product details: hydrOXYzine Hydrochloride Oral Solution, USP, 10 mg/5 mL, 473 mL (1 Pint), Rx only, Distributed by: ANI Pharmaceuticals, Inc., Baudette, MN...
- Company
- ANI Pharmaceuticals, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets. Product details: Perampanel CIII Tablets, 6mg, Rx only, 30...
- Company
- SUN PHARMACEUTICAL INDUSTRIES INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). Product details: Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.H1; burrs,...
- Company
- SURGIFY MEDICAL OY
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process. The sensors were later sold to pharmacies and...
- Company
- Dexcom, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). Product details: Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills,...
- Company
- SURGIFY MEDICAL OY
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. Product details: Off-Axis Comprehensive Shoulder System,...
- Company
- Zimmer, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm...
- Company
- Ventec Life Systems, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. Product details: Convenience kits...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for thrombus formation during prolonged use of the introducer. Product details: Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile...
- Company
- Abiomed, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). Product details: Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.125.NVG.H1; drills, burrs,...
- Company
- SURGIFY MEDICAL OY
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker...
- Company
- Philips North America Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). Product details: Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.U1; drills, burrs,...
- Company
- SURGIFY MEDICAL OY
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). Product details: Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.H1; drills, burrs,...
- Company
- SURGIFY MEDICAL OY
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister,...
- Company
- Medtronic Perfusion Systems
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. Product details: Off-Axis Alliance Glenoid, Right, 4-Peg,...
- Company
- Zimmer, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Marquesita de Chocolate y Vainilla [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Rollitos de Guava [image] Guava Rolls The Original, Net Wt. 15 oz, packaged in a transparent and rigid plastic...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Rollitos de DulceLeche [image] Caramel Rolls The Original, Net Wt. 15 oz, packaged in a transparent and rigid...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Cheesecake de Fresa [image] Strawberry Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Tiramisu [image] Cofee Cake The Original, Net Wt. 30 oz, packaged in a transparent and rigid plastic clamshell...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Marquesita de Mango [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Cake de Fresa y Chocolate [image] Stawberry & Chocolate Cake The Original, Net Wt. 48 oz, packaged in a rigid...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Cake de Mango [image] Mango Cake The Original, Net Wt. 47 oz, packaged in a rigid plastic clamshell container...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Cheesecake de Guava [image] Guava Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared FD&C Red 40 Product details: ESTRELLA, Bebida de Parcha (Passion Fruit Drink), multiple sizes, 14 OZ.FL. (413 ML), 64 OZ.FL (1,920mL), 120 OZ.FL. (3.54LT.) 14 OZ.FL Plastic...
- Company
- Refresqueria Estrella Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Potential physical contamination: dark spot was noticed on the bottom of container. Product details: MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, Cal/Oz: 19, 0.9 g/dL...
- Company
- Mothers' Milk Bank of Louisiana at Ochsner Baptist
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The product contains unapproved colors chlorophyll E140 and E141. Product details: .155 CRUNCHY CANNOLI GLUTEN FREE intended use: DESSERT condition: shelf stable shelf life: 12 month type...
- Company
- MID DOLCIARIA SRL
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared melatonin. Product details: Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies. Net weight: 11.36 ounces. Serving size: 2 gummies. UPC:...
- Company
- Dkiru LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Firm observed oily and sticky substance on direct food contact surface packaging of finished product. Product details: Great Value Hawaiian Roll 4pk, Item # F63384. Product is perishable...
- Company
- United States Bakery
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared fish. Product details: azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT OF JAPAN DISTRIBUTED BY: AZUMA FOODS INTERNATIONAL INC., U.S.A....
- Company
- Azuma Foods International Inc USA
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The product contains unapproved colors chlorophyll E140 and E141. Product details: CANNOLI SICILIANI intended use: DESSERT condition: shelf stable shelf life: 12 month type of packaging:...
- Company
- MID DOLCIARIA SRL
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Plain salt was labeled as iodized and iodized salt was labeled as plain. Product details: Salt
- Company
- United Salt Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product requires refrigeration but the label is missing a "Keep Refrigerated" statement Product details: Fairhope Roasting Company Cold Brew Coffee Concentrate, packaged in 1-gallon...
- Company
- Fairhope Roasting Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Allergen (Soy) Product details: Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow Wrapped, 48 units per case, Keep frozen
- Company
- Nutrisystem Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Defective container:may contain bottles with incomplete seals Product details: DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz. (30 g), Manufactured for and Distributed...
- Company
- Keystone Industries
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; deficiencies observed during FDA inspection Product details: Med Pride, HYDROCORTISONE CREAM 1%, Net Wt. 1 oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook...
- Company
- Dabur India Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Defective container:may contain bottles with incomplete seals Product details: PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor, Manufactured for Pure Life,...
- Company
- Keystone Industries
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; deficiencies observed during FDA inspection Product details: Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate 3.5 mg, Polymyxin-B...
- Company
- Dabur India Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; deficiencies observed during FDA inspection Product details: Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc (equivalent to 400 units), Neomycin Sulfate 5 mg,...
- Company
- Dabur India Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; deficiencies observed during FDA inspection Product details: Lucky Super Soft, First Aid Triple Antibiotic Ointment, Bacitracin zinc 400 units, neomycin sulphate 3.5 mg,...
- Company
- Dabur India Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; deficiencies observed during FDA inspection Product details: Med Pride, Bacitracin Zinc Ointment, 1oz (28.3g) per tube, 72 tubes per case, Manufactured for: Shield Line...
- Company
- Dabur India Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride, syringe, IntegraDose Compounding Services, LLC. 3650 Victoria St N, Suite 900, Shoreview, MN, NDC...
- Company
- IntegraDose Compounding Services LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Dissolution Specifications Product details: Chlorthalidone Tablets, USP, 25 mg, [100 or 1000] Tablets pr bottle, Rx only, Manufactured by: Inventia Healthcare Limited, Additional...
- Company
- Inventia Healthcare Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Defective container:may contain bottles with incomplete seals Product details: Quala Dental Products, Topical Anesthetic Gel, 20 % Benzocaine, Strawberry Flavor Net Contents: 1 oz (30 g),...
- Company
- Keystone Industries
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; deficiencies observed during FDA inspection Product details: Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes,...
- Company
- Dabur India Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; deficiencies observed during FDA inspection Product details: Med Pride, HYDROCORTISONE CREAM 1%, Net Wt. 16oz (454g) tubes, Manufactured for: Shield Line LLC, 59 Hook...
- Company
- Dabur India Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; deficiencies observed during FDA inspection Product details: Med Pride, Bacitracin Zinc Ointment, 500 units, 1oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook...
- Company
- Dabur India Limited
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 Product details: VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 50...
- Company
- PAI Holdings LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 Product details: VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 25...
- Company
- PAI Holdings LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware. Product details: Medtronic O-arm O2 Imaging System. Model Number: BI70002000.
- Company
- Medtronic Navigation, Inc.-Boxborough
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a product past its Use By Date may...
- Company
- Inspire Medical Systems Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of...
- Company
- ARROW INTERNATIONAL, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of...
- Company
- ARROW INTERNATIONAL, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical circulatory support. Product...
- Company
- Abiomed, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon...
- Company
- Howmedica Osteonics Corp.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application. Product details:...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of...
- Company
- ARROW INTERNATIONAL, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of...
- Company
- ARROW INTERNATIONAL, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application. Product details:...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to 11 volt Backup Battery failures. Product details: Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog Number: 106531US Software Version: N/A Product...
- Company
- Thoratec LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 1000 mg, 160-count bottle,...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility Product details: Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by: Spectra Medical Devices, LLC, Wilmington, Made in S....
- Company
- Spectra Medical Devices, Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: HyVee, Ultra Strength Antacid, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY:...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: CAREone, EXTRA STRENGTH CALCIUM ANTACID, Calcium Carbonate 750 mg, 96 chewable Tablets,...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with lead. Product details: DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz (125 g) PRODUCT OF THAILAND Packed for: U.S. Trading Company Hayward, CA 94545-1130...
- Company
- U.S. Tov, Inc. dba U.S. Trading Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Napolitano [image] Neapolitan The Original, Net Wt. 22 oz, packaged in a transparent and rigid plastic clamshell...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Cake de Capuchino [image] Capuchino Cake The Original, Net Wt. 63 oz, packaged in a transparent and rigid plastic...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May contain metal pieces Product details: Farm Rich Pizza Cheese Crunchers
- Company
- Rich Products Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste. Product details: NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC,...
- Company
- SENSORY SUPPLEMENT LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Cheesecake de Dulce de Leche [image] Caramel Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Imported Enoki Mushrooms tested positive for Listeria Monocytogenes. Product details: HH Fresh Trading Corp. (branded) ENOKI MUSHROOM; Premium Quality; Net WT/ Poids Net 150g(5.29oz)...
- Company
- HH FRESH TRADING CORP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Cake de Coco [image] Coconut Cake The Original, Net Wt. 47 oz, packaged in a rigid plastic clamshell container...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Cheesecake de Mango [image] Mango Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Jumbo Brazo Gitano Caramelo [image] Jumbo Caramel Roll The Original, Net Wt. 40 oz, packaged in a rigid plastic...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Brazo Gitano [image] Caramel Sweet Roll The Original, Net Wt. 24 oz, packaged in a rigid plastic clamshell...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40). Product details: Marquesita de Dulceleche [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent...
- Company
- Galaxy RG Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The ingredient, Pista, currently declared on our label should be corrected to the standard American nomenclature, Pistachio. Product details: WeiKFiELD Custard Powder Kesar Pista, Net Wt....
- Company
- Weikfield Foods Pvt. Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysis Product details: Minocycline Hydrochloride...
- Company
- Ascend Laboratories, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process. Product details: Gas-X Extra Strength, SIMETHICONE...
- Company
- Haleon US Holdings LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the ampoule solution Product...
- Company
- SUN PHARMACEUTICAL INDUSTRIES INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Microbial contamination of sterile products Product details: Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, Made in USA, A Zep Inc. Brand, Distributed by:...
- Company
- Zep Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit Product details: Duloxetine Delayed-Release Capsules, USP, 60mg, packaged in a) 90 Capsules...
- Company
- Breckenridge Pharmaceutical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Impurities/Degradations Specifications Product details: Epinephrine Injection, USP, 1mg/mL, 1 mL single-dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-696-02...
- Company
- Fresenius Kabi USA, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate matter: Particulate matter identified as glass. Product details: DOXOrubin Hydrochloride Liposome injection, 50 mg/25 mL (2mg/mL), 25 mL single-dose vials, Sterile,...
- Company
- SUN PHARMACEUTICAL INDUSTRIES INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Microbial Contamination of Non-Sterile Products Product details: BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL) per bottle,...
- Company
- BEEKEEPER'S NATURALS USA INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit Product details: Duloxetine Delayed-Release Capsules, USP, 30mg, 1000 Capsule bottles, Rx...
- Company
- Breckenridge Pharmaceutical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer. Product details: Primidone Tablets, USP, 50...
- Company
- Amneal Pharmaceuticals, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Dissolution Specifications: During 12-month long-term stability testing, subject lot was out of specification (low) for stage 3 dissolution at the 24-hour timepoint. Product...
- Company
- Golden State Medical Supply Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. Product details: Brand Name: CGuard¿ Prime Carotid...
- Company
- INSPIREMD Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock...
- Company
- GE Medical Systems, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
There is an error in the labeling of the GTIN on the product. When scanned; however, the case labeling, lot number, and printed labeling on the product correctly identifies the product...
- Company
- Fresenius Medical Care Holdings, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. Product details: Product Name: CORFLO* Safety PEG Kit with...
- Company
- Avanos Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. Product details: Product Name: MIC Safety Percutaneous...
- Company
- Avanos Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays. Product details: Mahurkar Elite PASS Trays; Description (Product...
- Company
- Mozarc Medical US LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. Product details: Product Name: MIC Safety Percutaneous...
- Company
- Avanos Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. Product details: Brand Name: CORFLO Product Name: CORFLO...
- Company
- Avanos Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. Product details: Brand Name: CGuard¿ Prime Carotid...
- Company
- INSPIREMD Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Reusable electrodes may not meet expected performance levels. Product details: Boston Scientific CSK Electrodes: REF: CSK-TC10, CSK Electrode, STAINLESS STEEL, 10 cm x 28 ga (0.36 mm) REF:...
- Company
- Boston Scientific Neuromodulation Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label. Product details: NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog...
- Company
- In2bones USA, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a multiple amplifier configuration (128...
- Company
- Micromed S.p.A.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Sterile anchors my lack sterility assurance. Product details: Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180
- Company
- Boston Scientific Neuromodulation Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Sesame Seeds White were labeled as Curry Powder Sweet. Product details: Lunds & Byerly's Curry Powder Sweet
- Company
- J and J Bunting, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with foreign objects (metal pieces). Product details: STRAUS FAMILY CREAMERY Cookie Dough ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed...
- Company
- Straus Family Creamery
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products may be potentially contaminated with Salmonella. Product details: White Cheddar Seasoning packaged in the following sized containers: 1. Net Wt. 1.2 oz (34g) Distributed by:...
- Company
- JCB Flavors, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination Product details: Aramark Cheese Sauce New & Improved, 25 lb., packaged in a...
- Company
- The Coffee Connexion Co., Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with foreign objects (metal pieces). Product details: STRAUS FAMILY CREAMERY Mint Chip ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by...
- Company
- Straus Family Creamery
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products may be potentially contaminated with Salmonella. Product details: Karlsburger Kitchens Garlic N Cheese Topper, Net Wt: 20 oz. (567g). Distributed by: Karlsburger Foods, Inc.,...
- Company
- JCB Flavors, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products may be potentially contaminated with Salmonella. Product details: #003020 Sour Cream & Onion, Net Wt: 10 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094.
- Company
- JCB Flavors, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Undeclared allergen (sesame). Ingredients panel does not list sesame as sub-ingredient of Za'atar spice and Contains statement does not declare sesame. Product details: Market of Choice...
- Company
- Market of Choice Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product does not meet label claim for Vitamin E. Product details: Yunker(branded) Energy & Health Herbal Supplement with Vitamins; Manufactured by Sato Pharmaceuticals Co. Ltd.; 30ml...
- Company
- Sato Pharmaceutical Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products may be potentially contaminated with Salmonella. Product details: #003740 Dill & Garlic Seasoning, Net Wt: 10 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094.
- Company
- JCB Flavors, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination Product details: 1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag...
- Company
- The Coffee Connexion Co., Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products may potentially be contaminated with Salmonella. Product details: ANGEL branded STRAWBERRY SOFT-SERVE powder; 10- 2-pound bag/case NO UPC.
- Company
- SKS Copack
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Salmonella. The firm was notified by the North Carolina Department of Agriculture that the product test positive for Salmonella. Product details: Malazi 100% PURE SUDANESE SESAME Tahina...
- Company
- Nassar Investment Company LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameters could not be verified. Product...
- Company
- Jesse Withrow
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Possible carbon steel foreign material (1-2mm) Product details: Betaine Anhydrous, 2055kg, material packed in foil bags inside 15kg cardboard box Label reads in part as "***BETAINE...
- Company
- Creative Compounds, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with foreign objects (metal pieces). Product details: STRAUS FAMILY CREAMERY Strawberry ORGANIC SUPER PREMIUM ICE CREAM ONE QUART (946mL) ONE PINT (473mL) Produced...
- Company
- Straus Family Creamery
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Un-eviscerated fish may be contaminated with clostridium botulinum Product details: Hellas Meze Golden Smoked Whole Herring
- Company
- Terra Medi LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products may be potentially contaminated with Salmonella. Product details: #0083004 Ranch Seasoning, Net Wt: 25 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094.
- Company
- JCB Flavors, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with foreign objects (metal pieces). Product details: STRAUS FAMILY CREAMERY Vanilla Bean ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed...
- Company
- Straus Family Creamery
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products may be potentially contaminated with Salmonella. Product details: #007560 Fiery Hot Seasoning (Reduced Salt), Net Wt: 25 lbs. JCB Flavors, 1224 Clark Street, Watertown, WI 53094
- Company
- JCB Flavors, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The product may contain undeclared allergens (cashews, pistachios), and dried cherries. Product details: SECOND NATURE KETO CRUNCH SMART MIX, 10-ounce retail-sized plastic pouch, UPC...
- Company
- SECOND NATURE BRAND
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products may be potentially contaminated with Salmonella. Product details: #009530 Ranch Seasoning, Net Wt: 50 lbs. JCB Flavors, 1224 Clark Street, Watertown, WI 53094.
- Company
- JCB Flavors, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products may be potentially contaminated with Salmonella. Product details: #800414/003729Butter Parsley, Net Wt: 50 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094
- Company
- JCB Flavors, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with Salmonella Product details: 72% CACAO CHOCOLATE WITH DATE SUGAR WAFERS Ingredients: Cacao Beans, Organic Date Powder, Organic Cocoa Powder Net Wt 25lb (11.3kg)...
- Company
- Guittard Chocolate Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: HyVee, Extra Strength Antacid, Calcium Carbonate 750 mg, 96 CHEWABLE TABLETS, DISTRIBUTED BY:...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan Product details: Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose...
- Company
- Eugia US LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: TopCare health, ULTRA STRENGTH, Antacid Tablets, CALCIUM CARBONATE 1000mg, 72 CHEWABLE...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: GOODSENSE Ultra Strength, Antacid TABLETS, Calcium Carbonate 1000 mg, 72 Chewable Tablets,...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 750 mg, 330-count bottle,...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: DISCOUNT drug mart, EXTRA STRENGTH, ANTACID TABLETS, Calcium Carbonate 750 mg, 96 Tablets,...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: CAREone, ULTRA STRENGTH CALCIUM ANTACID, Calcium Carbonate 1000 mg, 72 chewable Tablets,...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: EQUALINE ultra strength, antacid tablets, calcium carbonate 1000mg, 72 chewable tablets,...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: GOODSENSE Extra Strength, Antacid TABLETS, Calcium Carbonate 750 mg, 96 Chewable Tablets,...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of foreign substance: small metallic particles in chewable tablets. Product details: EQUALINE extra strength, antacid tablets, calcium carbonate 750mg, 96 chewable tablets,...
- Company
- Guardian Drug Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona Product details: Xyvona...
- Company
- SUN PHARMACEUTICAL INDUSTRIES INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the...
- Company
- B Braun Medical Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching...
- Company
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential...
- Company
- B Braun Medical Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Temperature probe devices lack FDA clearance. Product details: Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050
- Company
- Covidien LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use. Product details: Atlan...
- Company
- Draeger, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the...
- Company
- B Braun Medical Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Fingerprint scanner may overheat to a temperature to cause 1st degree burn. Product details: BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
- Company
- CareFusion 303, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock cannot be...
- Company
- Bayer Medical Care, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching...
- Company
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the...
- Company
- Intuitive Surgical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Fingerprint scanner may overheat to a temperature to cause 1st degree burn. Product details: BD Pyxis Mini Main REF: 349 Medication cabinet
- Company
- CareFusion 303, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face. Product details: Arvis Hip & Knee 3.0 Instrument Set, REF:...
- Company
- Kico Knee Innovation Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product was made with milk powder recalled by the supplier due to Salmonella contamination. Product details: Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113. Net Wt 25.00 lbs...
- Company
- PS Seasoning & Spices, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
potential presence of Salmonella Product details: Good & Gather Mexican Street Corn Trail Mix 8 oz bag UPC 085239270240, 8 bags per case
- Company
- JOHN B SANFILIPPO & SONS INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with Salmonella. Product details: GHIRARDELLI SWEET GROUND POWDER WHITE CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.41kg Distributed by Ghirardelli Chocolate...
- Company
- Ghirardelli Chocolate Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May be under-processed resulting in growth of Clostridium botulinum and lists health claims. Product details: Menopause Bully 16 oz and 32 oz.
- Company
- LIQUID BLENZ CORP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
potential to be contaminated with Salmonella Product details: Solina 6036195 Ranch Seasoning, 50lb bag
- Company
- Solina U.S. Holding
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product was made with milk powder recalled by the supplier due to Salmonella contamination. Product details: VG7274D1 Natural Cream of Mushroom Type Flavor, Net Weight: 50 lbs. bag. Item...
- Company
- Fontana Flavors, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
potential presence of Salmonella Product details: Fisher Tex Mex Trail Mix 30 oz plastic jar UPC 070690275941, 6 jars per case
- Company
- JOHN B SANFILIPPO & SONS INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. Product details: Liposomal Sleep Spray. Dosage: 6...
- Company
- Wellnov Supplements LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
potential to be contaminated with Salmonella Product details: Solina 6036443 Cheddar Cheese Powder Seasoning, 50lb bag
- Company
- Solina U.S. Holding
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product was made with milk powder recalled by the supplier due to Salmonella contamination. Product details: Blackstone Parmesan Ranch Seasoning, Net Wt 7.3 oz (207g). UPC 7 17604-04106 2....
- Company
- PS Seasoning & Spices, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. Product details: Liposomal B12 Spray. Dosage: 3 sprays...
- Company
- Wellnov Supplements LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with Salmonella. Product details: GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk ***...
- Company
- Ghirardelli Chocolate Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
potential to be contaminated with Salmonella Product details: Solina 6036087 Cr¿me Fraiche Spice Seasoning, 25lb bag
- Company
- Solina U.S. Holding
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
potential to be contaminated with Salmonella Product details: Solina 6036277 Garlic Cream Sauce Seasoning, 40lb bag
- Company
- Solina U.S. Holding
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. Product details: Liposomal Kids Liquid Multivitamin...
- Company
- Wellnov Supplements LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
potential to be contaminated with Salmonella Product details: Solina 6036554 Parmesan Breadstick Sauce Seasoning, 40lb bag
- Company
- Solina U.S. Holding
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule. Product details: Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip,...
- Company
- Safecor Health, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent Drug Product details: fentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compounding Services LLC, 3650 Victorie St N, Suite 900,...
- Company
- IntegraDose Compounding Services LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit Product details: Erythromycin Tablets, USP, 500 mg, 30 tablets per bottle, Rx...
- Company
- Zydus Pharmaceuticals (USA) Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of particulate matter: a white thread-like structure in the cartridge Product details: Liraglutide Injection, 18 mg/3 mL (6 mg/mL), Rx only, Manufactured for: Lupin...
- Company
- Lupin Pharmaceuticals Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit Product details: Erythromycin Tablets, USP, 250 mg, 30 tablets per bottle, Rx...
- Company
- Zydus Pharmaceuticals (USA) Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. Product details: Primidone Tablets, USP, 50 mg, 100 Tablets (10 x 10 unit dose blister) per...
- Company
- Amerisource Health Services LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. Product details: Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by:...
- Company
- Golden State Medical Supply Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. Product details: Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by:...
- Company
- Golden State Medical Supply Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus. Product details: MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%),...
- Company
- Wisconsin Pharmacal Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility Product details: cimzia (certolizumab pegol), 2x200mg/mL PREFILLED SYRINGES (2 single-dose), Rx ONLY, Manufactured by: UCB Inc., Smyrna, GA 30080, a) NDC...
- Company
- UCB Biosciences Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. Product details: Primidone Tablets, USP, 250 mg, 100 Tablets (10 x 10 unit dose blister) per...
- Company
- Amerisource Health Services LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Defective Container; packets were found to be either empty or partially full. Product details: Estradiol Gel, 0.1%, 0.25 mg, 0.25 g per packet, 30 packets per carton, Rx only, Distributed...
- Company
- ANI Pharmaceuticals, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Impurities/Degradation Specifications Product details: Busulfan Injection, 60 mg per 10 mL (6 mg per mL), 8x10 mL Single-Dose Vials, Rx only, Mfd. for Sagent Pharmaceuticals,...
- Company
- Sagent Pharmaceuticals
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an HDD may,...
- Company
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products were made with recalled California Dairies milk powder due to Salmonella. Product details: Butter Parsley Bagel Crisps, Item Number 18490, Net Weight: 10 lbs. Legacy Bakehouse,...
- Company
- Legacy Bakehouse LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Milk Allergen, Product details: Wawa Diet Iced Tea Lemon Pint (16oz),Plastic bottle
- Company
- Wawa Beverage Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Milk Allergen, Product details: Wawa Diet Lemonade Pint (16oz), Plastic bottle
- Company
- Wawa Beverage Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products. Product details: (BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item#...
- Company
- Honeyville, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products were made with recalled California Dairies milk powder due to Salmonella. Product details: giant eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps, Net Wt 7.33 oz....
- Company
- Legacy Bakehouse LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products were made with recalled California Dairies milk powder due to Salmonella. Product details: Parmesan & Herb Bagel Crisps, Item Number 18139, Net Weight: 10 lbs. Legacy Bakehouse,...
- Company
- Legacy Bakehouse LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Milk Allergen, Product details: Wawa Iced Tea Lemon 16 oz Pint, Plastic bottle
- Company
- Wawa Beverage Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Milk Allergen, Product details: Wawa Fruit Punch Pint (16oz), Plastic bottle
- Company
- Wawa Beverage Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Possible cross-contamination resulting in undeclared allergen ingredient (Peanut) Product details: Fly By Jing (branded) Creamy Sesame Noodles; 3.8 oz packets. Sold in single and 4 packs....
- Company
- Fly By Jing Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of individual units. Product...
- Company
- AVEVA Drug Delivery Systems, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Stability Specifications Product details: PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Allergen, Inc., an AbbVie company, North...
- Company
- AbbVie Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a...
- Company
- GE Medical Systems Information Technologies Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Retrospective submission for following issues identified: 1. Alarm failures, power-path faults, electrical-short risks, and inaccurate motor-current sensing were identified in certain AIC...
- Company
- Abiomed, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a...
- Company
- GE Medical Systems Information Technologies Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because the outer carton and blister...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Labeling update concerning proximal clasp disconnection from the outer control tube which may prevent stent graft from being released from the delivery system. Product details: RelayPro...
- Company
- Bolton Medical Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates. Product details: Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model...
- Company
- Medtronic Neuromodulation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Nitrile Exam Glove failed to meet specifications chemical permeation performance. Product details: Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772...
- Company
- O&M HALYARD INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May be under-processed resulting in growth of Clostridium botulinum and lists health claims. Product details: Fibroid Bully 16 oz and 32 oz.
- Company
- LIQUID BLENZ CORP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Seasoning was made with recalled California Dairies milk powder due to Salmonella contamination. Product details: Pork King Good Onion & Sour Cream Seasoning. Net Wt. 3 oz (85G) bottle....
- Company
- Pork King Good, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with Salmonella. Product details: GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX WHITE MOCHA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk ***...
- Company
- Ghirardelli Chocolate Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May be under-processed resulting in growth of Clostridium botulinum and lists health claims. Product details: Prostate Bully 16 oz and 32 oz
- Company
- LIQUID BLENZ CORP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May be under-processed resulting in growth of Clostridium botulinum and lists health claims. Product details: Blackseed Bitters 16 oz and 32 oz.
- Company
- LIQUID BLENZ CORP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
May be under-processed resulting in growth of Clostridium botulinum and lists health claims. Product details: Pure Shilajit Tonic 16 oz and 32 oz
- Company
- LIQUID BLENZ CORP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with Salmonella. Product details: GHIRARDELLI SWEET GROUND POWDER CHOCOLATE & COCOA NET WT 48oz (3lbs) 1.36kg Distributed by Ghirardelli Chocolate Company, San...
- Company
- Ghirardelli Chocolate Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. Product details: Liposomal Mens 50+ Liquid...
- Company
- Wellnov Supplements LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
potential to be contaminated with Salmonella Product details: Solina 6022487 Garlic Herb Topping, 50lb bag
- Company
- Solina U.S. Holding
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. Product details: Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by:...
- Company
- Lannett Company Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Labeling: Not Elsewhere Classified- Incomplete inactive ingredient information on the carton labeling. Product details: Gas-X, Simethicone 125 mg/ ANTIGAS, 120 SoftGels, Distributed by:...
- Company
- Haleon US Holdings LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood...
- Company
- Becton, Dickinson and Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Certain lots of product have the potential for a sterile barrier breach. Product details: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary...
- Company
- Medtronic Perfusion Systems
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Certain lots of product have the potential for a sterile barrier breach. Product details: Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T;...
- Company
- Medtronic Perfusion Systems
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood...
- Company
- Becton, Dickinson and Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control...
- Company
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the implant with the inserter, which...
- Company
- Novapproach Spine, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to stain present on the surface of affected foley catheters. Product details: Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic...
- Company
- C.R. Bard Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Affected devices exhibited fractures at the distal shaft tip without complete detachment. Product details: Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1)...
- Company
- TANGENT ENDOSCOPY, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may...
- Company
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Yellow #5 Product details: Banana Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00903
- Company
- Silver Moon LP dba Loard's Ice Cream
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Milk, Soy, Red #40. Product details: Loard's Peppermint Ice Cream - 32 oz; 56 oz
- Company
- Silver Moon LP dba Loard's Ice Cream
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with Salmonella. Product details: Low Heat Non-Fat Dried Milk Powder - paper bags 25 kg. (packed under 5 labels: Off Grade NFDM Variable; Extra Grade NFDM Standard...
- Company
- California Dairies Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Multi-state outbreak of E. coli O157:H7. Product details: RAW FARM RAW CHEDDAR SIMPLY SHREDDED Original MADE WITH: WHOLE RAW MILK TRULY RAW - NEVER WARMED ABOVE 102F MADE IN THE USA KEEP...
- Company
- Raw Farm LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Package integrity compromised. Product details: Horizon Organic Chocolate Organic Lowfat Milk. Saleable Unit UPC: 742365004322 (6-8 FL OZ Milk Boxes). Case: ORG MILK 1% DHA CHOCOLATE 3/6PK...
- Company
- Horizon Organic Dairy, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with foreign materials. Product details: LUNDBERG FAMILY FAMRS WHITE RICE JASMINE NET WT 32 OZ (2 lb) 907 g Manufactured and Distributed by: Lundberg Family Farms...
- Company
- Wehah Farms
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. Product details: Fain s Blackberry Honey Spread, 12oz net wt., UPC 01832213862
- Company
- Walker Honey Co
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Milk, Red #40. Product details: Loard's Champagne Sherbert - 32 oz
- Company
- Silver Moon LP dba Loard's Ice Cream
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with Salmonella. Product details: Low Heat Non-Fat Dried Milk Powder - plastic totes (NTE) 2200 lbs. (packed under 5 labels: Off Grade NFDM Variable; Grade A NFDM...
- Company
- California Dairies Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella. Product details: Costco Service Deli Department...
- Company
- Griffith Foods Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product has the potential to be contaminated with Salmonella. Product details: Bulk WN-976-782-1 Seasoning for Cheese Sauce, Net Wt. 43.50 lbs., in a brown kraft bag
- Company
- Givaudan Flavors Corp
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Incorrect Product Formulation: product did not contain insulin as listed in the label. Product details: TPN bag (patient specific), Rx# 11-4909703-0-1, Compound Volume 1660 mL per bag, Rx...
- Company
- Central Admixture Pharmacy Services, Inc (CAPS) Los Angeles
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals. Product details:...
- Company
- Ajanta Pharma Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Chemical contamination; presence of lead and lithium above specification Product details: NAPROXEN ORAL SUSPENSION, USP, 125 mg/5mL, Rx only, 16fl oz (473 mL) bottles, Distributed by:...
- Company
- Acella Pharmaceuticals, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Impurities/Degradation Specifications:Out of specification result occurred in Organic Impurities Test Product details: Enalapril Maleate Tablets, USP, 20 mg, 1,000-count bottle, Rx...
- Company
- JB Chemicals and Pharmaceuticals Ltd
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals. Product details:...
- Company
- Ajanta Pharma Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Subpotent drug Product details: busPIRone Hydrochloride Tablets, USP, 5 mg, 500-count bottle, Rx Only, Manufactured by Unichem Laboratories LTD., Ind, Area, Meerut Road, Ghazibad - 201...
- Company
- Unichem Pharmaceuticals USA Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit Product details: Duloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle, Mfr. by...
- Company
- Breckenridge Pharmaceutical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of Particulate Matter. Product details: Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07.
- Company
- B BRAUN MEDICAL INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility: Potential leaks from perforations in bags. Product details: DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for...
- Company
- Fresenius Medical Care Holdings, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer. Product details:...
- Company
- Teva Pharmaceuticals USA, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object (stainless steel dust/flakes or shreds of plastic) Product details: Dakota Honey Company Spreadable Spun Honey, Salted Caramel. Stir before use. Produced in Winner, SD....
- Company
- Dakota Honey Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may contain foreign objects, specifically glass. Product details: Alain MILLIAT; MARMELADE ORANGE; 300 g 10.6 oz; packaged in glass jars
- Company
- FINESALER LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Contains undeclared allergens (cashews, milk, and soy). Product details: Uncle Giuseppe's Marketplace Milk Chocolate Bridge Mix, 11 oz Net Wt, packed in clear tamper resistant plastic...
- Company
- WE R NUTS
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object (stainless steel dust/flakes or shreds of plastic) Product details: Dakota Honey Company Spreadable Spun Honey, Jalapeno. Stir before use. Produced in Winner, SD. Packaged...
- Company
- Dakota Honey Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Salmonella Product details: Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk; tea/food manufacturers. Closed container stored in a cool settings at ambient/room...
- Company
- Pure Ground Ingredients, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object (stainless steel dust/flakes or shreds of plastic) Product details: Dakota Honey Company the Honey Flight. 4 Flavors of Spreadable Spun Honey Original - Salted Caramel -...
- Company
- Dakota Honey Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Contains undeclared Blue 1 Product details: Swad Mango Flavored Masala Candy
- Company
- Raja Foods and Vegetables Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared allergens (wheat and soy). Product details: Frederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag NET WT 9 OZ (255g). On the back of the bag...
- Company
- Ferris Coffee and Nut Company, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due to possible salmonella. Product...
- Company
- Sugar Foods LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products contain undeclared soy, specifically soy lecithin. Product details: Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO popcorn, brown sugar,...
- Company
- Prospector Popcorn, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object (stainless steel dust/flakes or shreds of plastic) Product details: Dakota Honey Company Spreadable Spun Honey, Cinnamon-Infused. Stir before use. Produced in Winner, SD....
- Company
- Dakota Honey Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Contains undeclared FD&C Yellow 6 Product details: Swad Orange Flavored Masala Candy
- Company
- Raja Foods and Vegetables Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared allergen ingredient (fish) Product details: ...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz UPC- 8651200409...
- Company
- Ocinet, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object (stainless steel dust/flakes or shreds of plastic) Product details: Dakota Honey Company Spreadable Spun Honey, Original. Stir before use. Produced in Winner, SD. Packaged...
- Company
- Dakota Honey Company
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision. Product details:...
- Company
- Oasis Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Presence of particulate matter: identified as Buprenorphine free base Product details: Buprenorphine Hydrochloride, Injection, 0.3mg/mL, 5x1 mL Single Dose Vials, Rx only, Manufactured...
- Company
- ENDO USA, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Dissolution Specifications Product details: Ascend Laboratories, LLC, Metoprolol Succinate Extended-Release Tablets, USP, 25 mg* Rx Only, Manufactured by: Alkem Laboratories Ltd.,...
- Company
- Ascend Laboratories, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified the presence of particulate within the fluid path of the Manifolds. Product details: Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain...
- Company
- GE Medical Systems, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Incomplete seals on sterile product Product details: BARD Dynamic Tip Steerable, Product Number 6DYNTP001;
- Company
- Stryker Sustainability Solutions
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is oversized may lead to...
- Company
- MICROVENTION INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to broken connector which may result in a temporary interruption of prescribed cold therapy. Product details: Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog...
- Company
- DJO, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Incomplete seals on sterile product Product details: BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Company
- Stryker Sustainability Solutions
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Complaints have been received of systems developing loose, missing, or broken internal bolts over time. Product details: SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers:...
- Company
- Hologic, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for mislabeled syringe produced by the i.v.STATION device. Product details: Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE,...
- Company
- Omnicell, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Incomplete seals on sterile product Product details: Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Company
- Stryker Sustainability Solutions
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain...
- Company
- GE Medical Systems, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified the presence of particulate within the fluid path of the Manifolds. Product details: Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107;...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to...
- Company
- Medtronic Neuromodulation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Incomplete seals on sterile product Product details: BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Company
- Stryker Sustainability Solutions
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Incomplete seals on sterile product Product details: Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Company
- Stryker Sustainability Solutions
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer. Product details: Similasan, iVIZIA, Sterile...
- Company
- Thea Pharma, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with pesticides, haloxyfop and thiamethoxam Product details: SunRidge Farms Organic CHILI BEAN BLEND CERTIFIED ORGANIC BY QAI NET WT. 15 LBS Item: 003056 UPC:...
- Company
- Falcon Trading Co., Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Soy (with mitigating circumstances) Product details: Chocolate Showers Ice Cream - 32 oz (5 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods, and Berkeley...
- Company
- Silver Moon LP dba Loard's Ice Cream
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Milk, Wheat, Soy, Yellow #5, Green #3. Product details: Loard's Lime Sherbert - 32 oz
- Company
- Silver Moon LP dba Loard's Ice Cream
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Milk, Walnuts, Eggs, Wheat, Soy. Product details: Loard's Brownie Nut Fudge Ice Cream - 32 oz
- Company
- Silver Moon LP dba Loard's Ice Cream
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Red #40, Blue #1, Blue #2 Product details: Burgundy Cherry Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00909
- Company
- Silver Moon LP dba Loard's Ice Cream
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Milk, Eggs, Yellow #5. Product details: Loard's Lemon Chiffon Ice Cream - 32 oz
- Company
- Silver Moon LP dba Loard's Ice Cream
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Milk, Red #3, Red #40, Blue #1, Blue #2. Product details: Loard's Ube Ice Cream - 32 oz
- Company
- Silver Moon LP dba Loard's Ice Cream
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
The potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm Product details: Garland Fresh Peeled Garlic 6 oz. bag
- Company
- Tops Markets LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Red #40 Product details: Peppermint Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00933
- Company
- Silver Moon LP dba Loard's Ice Cream
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. Product details: Natural Creamed Honey, 671333101377 *These product labels may...
- Company
- Walker Honey Co
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. Product details: Lemon Creamed Honey, 671333101353 *These product labels may...
- Company
- Walker Honey Co
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. Product details: Blackberry Creamed Honey 671333101308 * These product labels...
- Company
- Walker Honey Co
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared Milk, Almonds, Soy, Sulfites. Product details: Loard's Almond Joy Ice Cream - 32 oz
- Company
- Silver Moon LP dba Loard's Ice Cream
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential contamination with pesticides, haloxyfop and thiamethoxam Product details: SunRidge Farms Organic Black Beans CERTIFIED ORGANIC BY QAI NET WT. 25 LBS. ORIGEN: ARGENTINA...
- Company
- Falcon Trading Co., Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals. Product details:...
- Company
- Ajanta Pharma Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold. Product...
- Company
- AVID Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The devices were distributed without required FDA premarket clearance or approval. Product details: One Step K in vitro diagnostic test REF: 81A4
- Company
- DFI Co., Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm. Product...
- Company
- Centinel Spine, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the inability...
- Company
- Physio-Control, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between the...
- Company
- American Contract Systems Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester). Product details: Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module...
- Company
- Spacelabs Healthcare, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared hazelnut and soy lecithin. Product details: Kirkland Signature Traditional Madeleines 12 Count/net wt. 18oz., Item #2000012, UPC 000020000127. Plastic clamshell container is...
- Company
- Costco Wholesale Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Lead level was higher than NYSAGM Standard. Product details: Spice Powder, 4 oz, Plastic Bag
- Company
- Summit Import Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40 Product details: Bombay Kitchen brand Punjabi Mix; Net Wt 9oz (255g); INGREDIENTS: Chickpea Flour, Water, Non-GMO...
- Company
- Ethnic Foods Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared milk. Product details: Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 042743-19015-0 Item: 100547
- Company
- Marquez Brothers International, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may be contaminated with Salmonella. Product details: SALUTE SEASONINGS; Ground All Spice; Net Wt 16oz; Unistel Industries 650 Blossom Road Rochester, NY 14610; UPC: 7 69203 01617 0
- Company
- Unistel Industries Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared milk. Product details: EL MEXICANO agua fresca de horchata Instant Horchata Drink NET WT 12oz (340g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY...
- Company
- Marquez Brothers International, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared milk. Product details: EL MEXICANO horchata casera Instant Horchata Drink NET WT 14oz (396g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY MARQUEZ...
- Company
- Marquez Brothers International, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Hard corn starch lumps were found in the product Product details: CHIPS AHOY! Baked Bites Brookie .22.4 oz Carton ( 2.8 oz pouch ) and 7.7 oz Carton ( 1.4 oz pouch)
- Company
- Mondelez Global Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Ingredients statement declares Anchovy and Sasame, but Contains statement does not declare Fish (Anchovy) and Sesame. Product details: Booey's Dragon's Breath sauce, 15.2oz ringneck glass...
- Company
- Booey's Gourmet LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
High sugar content. The firm was notified by the FDA that sample results were positive for a high C4 sugar content. Product details: Raw & Unfiltered Bee Well Wildflower Honey NET wT. 12...
- Company
- Bee Well Honey Farm & Supply Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
mislabeled Coconut Date Bites. (product is coconut covered, label is for regular date bites) Product details: Label is predominantly green with white lettering in a clear plastic clamshell...
- Company
- PURE PALM C/O DVD
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
May be temperature abused, which may result in growth of Clostridium botulinum Product details: Crab Cakes various sizes sold to food service
- Company
- Connecticut Crab Company LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Contains undeclared FD&C Yellow 6 Product details: Negita Cracker- Shrimp 2.8oz
- Company
- Hadson (Toko) Trading Co. Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40). Product details: 52USA brand POPPING BOBA; PASSION...
- Company
- Guangdong Zonegoing Food Co., LTD
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40). Product details: 52USA brand POPPING BOBA; MANGO...
- Company
- Guangdong Zonegoing Food Co., LTD
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may contain foreign objects, specifically glass. Product details: Specially SELECTED brand Vanilla Creme Brulee; NET WT 3.6oz (103g); INGREDIENTS: CREAM (MILK, CREAM), FROZEN YOLK...
- Company
- LACTALIS CANADA, INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Undeclared allergen (almond). Product details: Top Lid Label: Einstein Bros Bagels Honey Almond Double-Whipped Shmear. Cup Label: Plain Whipped Cream Cheese Spread. Net Wt 6 oz (170g). UPC...
- Company
- Schreiber Foods Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40). Product details: 52USA brand POPPING BOBA;...
- Company
- Guangdong Zonegoing Food Co., LTD
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Foreign object found inside retail container. Product details: My Mochi Strawberry flavored Non-Dairy Frozen Dessert; 7.5 oz; 6 pieces per container. UPC# 0-70934-99645-8
- Company
- The Mochi Ice Cream Company, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product contains undeclared Yellow No. 5. Product details: Calypso Tropic Tango Lemonade. 16 FL oz (1PT) (473 ML). UPC 0 79581-18709 7. Keep Refrigerated After Opening. King Juice Company,...
- Company
- King Juice Company, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Undeclared food colorings (Yellow 6, Blue 1, and Yellow 5) and unapproved Acid Red 14. Product details: KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm, 818812022208,...
- Company
- Ganesha Enterprises LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
product tested positive for Listeria Monocytogenes. Product details: Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, 150g clear plastic package; Product of Korea, Keep...
- Company
- HEMU TRADING INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
cGMP deviations. Product details: Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31.
- Company
- Wells Pharma of Houston LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer. Product details: iVIZIA, Sterile Lubricant...
- Company
- Thea Pharma, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
cGMP deviations. Product details: fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 1000 mcg/50mL (20 mcg per mL), well pharma of Houston, NDC 73702-203-65.
- Company
- Wells Pharma of Houston LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
cGMP deviations. Product details: fentaNYL Citrate injectable Solution in 0.9% Sodium Chloride, Narcotic, (2500 mcg/ 250 mL) (10 mcg per mL), 250 mL bag, wells pharma of Houston, NDC...
- Company
- Wells Pharma of Houston LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality. Product details: GenTeal Tears, Lubricant Eye Gel, Sterile, 10g (0.34 Fl...
- Company
- Alcon Research LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
This recall is being conducted due to out of specification assay results in a limited number of bottles that were stored on side. Product details: Alendronate Sodium Oral Solution, 70...
- Company
- Hikma Pharmaceuticals USA INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
cGMP deviations. Product details: fentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, Wells Pharma in Houston, NDC 73702-202-02.
- Company
- Wells Pharma of Houston LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility Product details: Optase Dry Eye Intense Drops (Glycerin 0.2%), packaged in 0.33 fl oz, Sterile, Manufactured for Scope Health Inc., 79 Madison Ave., 8th...
- Company
- SCOPE HEALTH
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
cGMP deviations. Product details: fentaNYL Citrate Injectable Solution, Narcotic, CII, 1250 mcg/25mL (50 mcg per mL), 25 mL, wells pharma of Houston, NDC 73702-204-25.
- Company
- Wells Pharma of Houston LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed PH Specifications Product details: Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One...
- Company
- Water-Jel Technologies, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality. Product details: Systane, Lubricant Eye Gel, Night Gel, Sterile, 10g (0.35...
- Company
- Alcon Research LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
cGMP deviations. Product details: Phenylephrine Hydrochloride Injectable Solution, 40mg, 250*mL Bag, wells pharma of Houston, NDC 73702-122-03
- Company
- Wells Pharma of Houston LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Labeling: Missing Label Product details: Levocarnitine Injection, USP, 1 g/5 mL (200 mg/mL), 5 mL Single-Dose Vial, For intravenous use, Rx Only, American Regent, Inc., Shirley, NY 11967....
- Company
- American Regent, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
cGMP deviations. Product details: fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 50 mcg/5mL)(10 mcg per mL), wells pharma, NDC 73702-202-15.
- Company
- Wells Pharma of Houston LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below...
- Company
- Becton Dickinson & Co.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
It was identified that certain devices were being operated outside the validated and FDA-cleared display configuration due to user modification of the manufacturer-installed settings....
- Company
- Hologic, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel...
- Company
- Philips North America
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Updated software, Brady software maintenance release 6 (SMR6), is now available for the ACCOLADE" family of pacemakers and cardiac resynchronization therapy pacemakers (CRT-Ps)1 and the...
- Company
- Boston Scientific Corporation
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Cyber vulnerability of BLE communication was found by CISA VDP program. Product details: WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor...
- Company
- WHILL, INC.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
ventricular fibrillation (VF) during radiofrequency (RF) therapy with the Medtronic Sphere-9 catheter in patients who have a Biotronik Implantable Cardioverter Defibrillator (ICD) or...
- Company
- Medtronic, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel...
- Company
- Philips North America
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Label declares cream cheese but does not declare milk Product details: Riverence Smoked Trout Dip, net wt. 7oz. Product is perishable, refrigerated, packaged in plastic tub. Product is...
- Company
- Riverence Provisions LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
FDA analysis revealed the presence of undeclared sildenafil Product details: Blue Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage:...
- Company
- Pure Vitamins and Natural Supplements, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Products contain banned sweetener: cyclamates. Product details: DADI NONGFU DRIED SALT CHILLI VEGETABLE(S); Ingredients: Radish, chili, roasted sesame, prickly ash, edible salt, soybean...
- Company
- MEI YU CHENG DA TRADING INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
FDA analysis revealed the presence of undeclared sildenafil Product details: Red Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage:...
- Company
- Pure Vitamins and Natural Supplements, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Products contain banned sweetener: cyclamates. Product details: Olive Skewers individually wrapped and packaged in clear plastic bag; 500g; INGREDIENTS: Olive, edible salt, white sugar,...
- Company
- MEI YU CHENG DA TRADING INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Potential Salmonella Contamination Product details: Fresh Cantaloupe (Whole, Fresh), brand name Ayco, wrapped in food safe plastic bags packed in corrugated cardboard cartons; 6-12 melons...
- Company
- AYCO FARMS INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
FDA analysis revealed the presence of undeclared sildenafil and Tadalafil Product details: Boner Bears Honey Male Enhancement 100% Wildflower Honey, total of 15 pouches per box, Net Wt 15...
- Company
- Pure Vitamins and Natural Supplements, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Monitoring
FDA
Official source
Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame. Product details: ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich, perishable, Keep...
- Company
- F&S Fresh Foods, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Contains undeclared egg, soy, and hazelnut Product details: Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count bottles
- Company
- Blueroot Health, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells. Product details: Omega-3-Acid, Ethyl Esters,...
- Company
- The Harvard Drug Group LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. Product details: DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B....
- Company
- B BRAUN MEDICAL INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit. Product details: Furosemide Tablets, USP, 80 mg, 100 Tablets bottles, Rx only, Manufactured by:...
- Company
- Leading Pharma, LLC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that...
- Company
- Premier Dental Products Co
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. Product details: LACTATED RINGER'S IRRIGATION, 3000 mL bags, Sterile, Ex only, B....
- Company
- B BRAUN MEDICAL INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin Product details: Claravis (isotretinoin capsule, USP), 10 mg, Packaged as a) 100-count...
- Company
- Teva Pharmaceuticals USA, Inc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. Product details: 0.9 % SODIUM CHLORIDE IRRIGATION, USP, 3000 mL bags, Rx only,...
- Company
- B BRAUN MEDICAL INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. Product details: Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy...
- Company
- B BRAUN MEDICAL INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots." Product details: Pantoprazole Sodium, Delayed-Release...
- Company
- Hetero Labs Limited (Unit V)
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing. Product details: Fluocinonide, USP, 0.05% Cream,...
- Company
- SUN PHARMACEUTICAL INDUSTRIES INC
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on...
- Company
- Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Chemical contamination: Presence of benzene Product details: FHF Farmhouse Fresh, Midnight Clearing, NIGHT LOTION, 2.5% BENZOYL PEROXIDE ACNE TREATMENT, OTC a) 0.5 fl. oz./15ml; and b)1...
- Company
- Owen Biosciences Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on...
- Company
- Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on...
- Company
- Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Product details:...
- Company
- Angiodynamics, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. Product details: Medline Kits: 1) HEART TRANSPLANT BIOPSY, Model...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Unapproved design changes to the products outside of the 510(k) clearance. Product details: Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes GU...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for detachment of a distal tip component of the device during use. Product details: Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 45cm. Model Number: TB2-0545FC.
- Company
- Olympus Corporation of the Americas
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. Product details: Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Product details:...
- Company
- Angiodynamics, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
XXX Product details: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115.
- Company
- Olympus Corporation of the Americas
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. Product details: LSL Healthcare Wound Closure Tray,...
- Company
- LSL Healthcare Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. Product details: Medline Kits: 1) CATH LAB CDS, Model Number:...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. Product details: Medline Kits: 1) ANGIOGRAPHY PACK-LF, Model...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Product details:...
- Company
- Angiodynamics, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. Product details: LSL Healthcare, Foley Urine...
- Company
- LSL Healthcare Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration