Halyard EYE PACK
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
- Agency
- FDA Device
- Recall date
- May 7, 2026
- Status
- Ongoing
- Company
- AVID Medical, Inc.
1. What product was recalled?
Halyard EYE PACK
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Quantity: 260 kits
Code or lot text: Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027).
- LOT
- 1680590 (6/30/2027).
- LOT
- Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026)
- RECALL-NUMBER
- Z-2763-2026
2. Is my exact product affected?
Compare every printed identifier. A matching value can indicate that your product is included.
3. What is the hazard?
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
4. What should I do now?
Follow the FDA recall notice and contact the recalling company for current instructions.
5. Where was it sold or distributed?
Nationwide
View source evidence for state distribution
- California: US Nationwide distribution in the state of California.
6. Were injuries or illnesses reported?
No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.
7. What remedy is available?
Follow the FDA recall notice and contact the recalling company for current instructions.
8. Is the recall active or closed?
The source status is Ongoing. Recall Index urgency is elevated, which is a separate deterministic site label.
9. When was the information checked?
Last checked .
- created
10. Where is the official source?
Open the official FDA Device source
Recall Index normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.