AVID Medical, Inc. recalls Halyard EYE PACK.
- Recalling company
- AVID Medical, Inc.
- Product
- Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
- Reason
- Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 7, 2026
- Reported
- Jul 29, 2026
- Distribution
- US Nationwide distribution in the state of California.
- Status
- Ongoing
- Quantity
- 260 kits
- Lot / codes
- Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027).
- Company location
- Toano, VA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2763-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2763-2026 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.