AVID Medical, Inc.: Device Recall
Recall #Z-2530-2025 · 08/04/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2530-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- AVID Medical, Inc.
- Status
- Ongoing
- Date Initiated
- 08/04/2025
- Location
- Toano, VA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 57 units
Reason for Recall
Potential for open header bag seals, compromising sterility.
Product Description
Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit.
Distribution Pattern
US Nationwide distribution in the state of Florida.
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.