FDAClass IIJuly 29, 2026

Halyard EYE PACK recall

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

Why was Halyard EYE PACK recalled?

Incorrect concentration of Betadine solution contained within certain AVID convenience kits.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Recalling firm
AVID Medical, Inc.
Quantity
260 kits
Distribution
US Nationwide distribution in the state of California.
Recall date
July 29, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls