AVID Medical, Inc.: Device Recall
Recall #Z-1001-2026 · 11/11/2025
Class I: Dangerous
Recall Details
- Recall Number
- Z-1001-2026
- Classification
- Class I
- Product Type
- Device
- Recalling Firm
- AVID Medical, Inc.
- Status
- Ongoing
- Date Initiated
- 11/11/2025
- Location
- Toano, VA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 52 units
Reason for Recall
Devices are not suitable for organ transplant.
Product Description
Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
Distribution Pattern
US Nationwide distribution in the states of FL, GA and Puerto Rico.
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.