Z-2763-2026 Class II Ongoing
FDA device recall Z-2763-2026 was initiated by AVID Medical, Inc. on May 7, 2026 and is designated Class II. Reason for recall: Incorrect concentration of Betadine solution contained within certain AVID convenience kits. The recall status is ongoing. Affected quantity: 260 kits.
Recall Details
- Product Type
- Devices
- Report Date
- July 29, 2026
- Initiation Date
- May 7, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 260 kits
Product Description
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Reason for Recall
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Distribution Pattern
US Nationwide distribution in the state of California.
Code Information
Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027).