FDA Medical devices recall ·
Halyard EYE PACK. Model recall
- Recall number
- Z-2763-2026
- Date
- (initiated May 7, 2026)
- Company / brand
- AVID Medical, Inc.
9000 Westmont Dr, Toano, VA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 260 kits
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Why was it recalled?
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027).
Distribution
US Nationwide distribution in the state of California.
States: California
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2763-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.