Is AVID Medical, Inc. recalled?

Yes — a recall has been published. Reason: Incorrect concentration of Betadine solution contained within certain AVID convenience kits.

TemporaryFDAOngoing

Can cause harm that is usually temporary.

Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.

Check the device or its packaging for

Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027).

Why: Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Distributed: US Nationwide distribution in the state of California.
Company: AVID Medical, Inc.
Announced: 29 July 2026This is the date the recall was announced. A company may have started it weeks earlier.
Recall began: 7 May 2026

Source: FDA record Z-2763-2026 · retrieved 20 July 2026

Every recall is shown word for word from the FDA and USDA, with a link to the source.