Recall Weekly
Moderate riskFDA DeviceClass II

Halyard EYE PACK convenience kit recalled for incorrect Betadine solution concentration

Certain Halyard EYE PACK convenience kits (Model LVEY27) contain Betadine solution at an incorrect concentration. The kits were distributed nationwide, primarily in California. No injuries have been reported.

From the FDA notice · Read the official notice ↗ · All AVID Medical recalls

What to do

  1. Check if you have a Halyard EYE PACK (Model LVEY27) with lot number 1680076 or 1680590.
  2. Do not use the kit if you have one of the affected lots.
  3. Contact your supplier or AVID Medical for instructions on return or replacement.
Official notice ↗

Is yours affected?

Compare your label or packaging with the recalled product.

Product
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Sold in
Nationwide
Made for
Adults (0 months and older)

Details

Units affected
260 kits
Illnesses reported
None reported
Manufactured in
9000 Westmont Dr, N/A, Toano, VA, United States
Classification
Class II
Recall number
Z-2763-2026

In the FDA's words

Description
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit. Incorrect concentration of Betadine solution contained within certain AVID convenience kits. Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027). Distribution: US Nationwide distribution in the state of California. Affected quantity: 260 kits
Hazard
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.

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