Drug recall
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
FDA recall event 99249 · Class II · AVID Medical, Inc.
Key facts
| Event ID | 99249 |
|---|---|
| Recall numbers | Z-2763-2026 |
| Recalling firm | AVID Medical, Inc. |
| Product type | Devices |
| Products | Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrect concentration of Betadine solution contained within certain AVID convenience kits. |
| Initiation date | May 7, 2026 |
| Report date | Jul 29, 2026 |
| City | Toano |
| State | VA |
| Country | United States |
| FEI number | 1047429 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: