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
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
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
Lack of assurance of Sterility: potential product contamination Product details: BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile...
- 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-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