Company page
AVID Medical, Inc. alerts
Verified recalls, refunds, lawsuits, and settlements involving AVID Medical, Inc..
Recall
Active
FDA
Official source
Product may be potentially contaminated with a lubricant used during the manufacturing process. Product details: ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;
- Company
- AVID Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Product may be potentially contaminated with a lubricant used during the manufacturing process. Product details: ADULT HEART TRAY SHANDS JACKS; Model/Item Number (Kit): SHND419-08;
- Company
- AVID Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. Product details: Haylard 18G SINGLE SHOT EPI...
- Company
- AVID Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal...
- Company
- AVID Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to...
- Company
- AVID Medical, Inc.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to...
- Company
- AVID Medical, Inc.
- 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
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
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
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