AVID Medical, Inc.: Device Recall
Recall #Z-1742-2025 · 03/31/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1742-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- AVID Medical, Inc.
- Status
- Ongoing
- Date Initiated
- 03/31/2025
- Location
- Toano, VA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 60 units
Reason for Recall
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
Product Description
Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.
Distribution Pattern
US Nationwide distribution in the states of IL & LA.
Other Recalls by AVID Medical, Inc.
- Class II: Risk 11/14/2025
- Class II: Risk 11/14/2025
- Class II: Risk 11/14/2025
- Class II: Risk 11/14/2025
- Class II: Risk 11/14/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.