Halyard EYE PACK — Class II medical device recall Z-2763-2026
Ongoing recall by AVID Medical, Inc., reported 2026-07-29, distributed nationwide. Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
| Recall number | Z-2763-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | AVID Medical, Inc., Toano, VA, United States |
| Recall initiated | 2026-05-07 |
| Classified | 2026-07-20 |
| Reported by FDA | 2026-07-29 |
| Distributed | Nationwide (US) |
| Quantity | 260 kits |
| UPC / GTIN / UDI-DI | 10809160499528 |
| Lot numbers | 1680076, 1680590 |
| Model numbers | LVEY27 |
Product
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Reason for recall
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2763-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.