AVID Medical, Inc. recalls Halyard
- Recalling company
- AVID Medical, Inc.
- Product
- Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
- Reason
- Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 30, 2026
- Reported
- Jun 17, 2026
- Distribution
- US Nationwide distribution in the state of Iowa.
- Status
- Ongoing
- Quantity
- 60 kits
- Lot / codes
- Kit Code: UIEB48-01. UDI-DI: 10809160484098. Lot Number: UIEB48-01. Expiration Date: 8/7/2028.
- Company location
- Toano, VA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2410-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2410-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.