AVID Medical, Inc.: Device Recall
Recall #Z-0443-2025 · 09/20/2024
Class II: Risk
Recall Details
- Recall Number
- Z-0443-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- AVID Medical, Inc.
- Status
- Ongoing
- Date Initiated
- 09/20/2024
- Location
- Toano, VA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 33 eaches
Reason for Recall
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
Product Description
Halyard PACEMAKER DRAPE - Medical convenience kits Model Number: VAST020-06
Distribution Pattern
US Nationwide distribution.
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.