FDA recall, , Moderate risk
AVID Medical Halyard Eye Pack Convenience Kit
The Halyard Eye Pack Convenience kit contains an incorrect concentration of Betadine solution.
Summary by Recall Canary from the FDA notice
What happened
AVID Medical, Inc. of Toano, Virginia recalled the Halyard EYE PACK convenience kit because it contains an incorrect concentration of Betadine solution. The recall began May 7, 2026, and was added to the FDA's Enforcement Report on July 20, 2026, with classification on the same date. The recall affected 260 kits distributed in California.
The FDA's weekly enforcement report listed the recall on July 29, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the model number, UDI-DI and lot code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Halyard Eye Pack
- Model number
- LVEY27
- UDI-DI
- 10809160499528
- Lot code
- 1680076
- 1680590
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the state of California.
- Company
- AVID Medical, Inc.Toano, Virginia
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99249
- Recall number
- Z-2763-2026
- Quantity recalled
- 260 kits
All recalls from AVID Medical, Inc.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
