Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
FDA Recall Z-2763-2026 · Posted 2026-07-20
Recalling FirmAVID Medical, Inc.
Recall StatusOpen, Classified
Product CodeOJK
Date Initiated2026-05-07
Product Quantity260 kits
Reason for Recall
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Firm Action
AVID Medical notified the single consignee on about 05/07/2026 via email. The consignee was instructed to identify, segregate, and quarantine all impacted products, add the provided warning labels to affected AVID kits to ensure all users are aware of the issue, and discard all impacted components upon opening the Eye Pack. Customers and end users were instructed that if they received affected products from a distributor, to please contact that distributor of sales representatives with questions. Distributors were instructed that if any of the affected kits identified were further distributed, to ensure all end-users are appropriately notified and maintain records of effectiveness. Recipients were requested to complete and return the provided Recall Response Form by 05/22/2026.
Root Cause
Process control
Distribution Pattern
US Nationwide distribution in the state of California.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.