- Recalling firm
- AVID Medical, Inc.
- Reason for recall
- Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- Affected products (lot / model / serial)
- Kit Code: AMPK48-01. UDI-DI: 10809160472798. Lot Number: 334669. Expiration Date: 8/27/2028.
- Units affected
- 120 kits
- Distribution pattern
- US Nationwide distribution in the state of Iowa.
- Firm location
- Toano, VA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2407-2026
- Recall initiated
- April 30, 2026
- FDA classification date
- June 11, 2026
- FDA report date
- June 17, 2026
- FDA event ID
- 99021
- Last updated on HTM Vibe
- July 23, 2026