Recall Ledger

Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit. recall (AVID Medical, Inc.)

Medical deviceClass IIOngoing

Summary: AVID Medical, Inc. is recalling Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.. Reason: Incorrect concentration of Betadine solution contained within certain AVID convenience kits.

What is being recalled

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

Why

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

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide distribution in the state of California. (states named: California)

How to tell if yours is affected

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

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-2763-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedMay 7, 2026
ReportedJuly 29, 2026
CompanyAVID Medical, Inc.
Company locationToano, VA, United States
Initiated byVoluntary: Firm initiated
Quantity260 kits

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Official FDA record