FDA Device recall Z-2763-2026
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit
- FDA Device
- Class II
- ongoing
- Published 2026-07-29
On 2026-07-29 the FDA classified a Class II recall of Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit by Avid Medical, citing incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2763-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-05-07 |
| Published | 2026-07-29 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Avid Medical |
| Distribution | US |
Product
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Reason
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Identifiers
| code_info | Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027). |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2763-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.