Recall Z-2410-2026
AVID Medical, Inc. · initiated April 30, 2026
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
Codes / lots: Kit Code: UIEB48-01. UDI-DI: 10809160484098. Lot Number: UIEB48-01. Expiration Date: 8/7/2028.
Reason for recall
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
FDA-determined cause: Process control
Action taken
AVID Medical notified consignees on about 04/30/2026 via emailed letter. Consignees were instructed to identify, segregate and quarantine all affected units on hand, discard all impacted kits and complete and return the provided Response Form. Distributors were instructed to ensure all end-users are appropriately notified and maintain records of effectiveness.
Details
- Recall number
- Z-2410-2026
- Initiated
- April 30, 2026
- Posted by FDA
- June 11, 2026
- Product code
- OJH – Orthopedic Tray
- Quantity
- 60 kits
- Distribution
- US Nationwide distribution in the state of Iowa.
- Recalling firm
- AVID Medical, Inc., Toano, VA
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-2407-2026 Class II | Halyard, Pain Pack. Kit Code: AMPK48-01.Inadvertent distribution of sealed pouches that had not undergone validated sterilization. | 04/30/2026Open, Classified |
| Z-2408-2026 Class II | Halyard, Towel Six Pack. Kit Code: AMTS70-01.Inadvertent distribution of sealed pouches that had not undergone validated sterilization. | 04/30/2026Open, Classified |
| Z-2409-2026 Class II | Halyard, Drape Pack. Kit Code: LMDP36-01.Inadvertent distribution of sealed pouches that had not undergone validated sterilization. | 04/30/2026Open, Classified |