FDA-Device2026-07-29Class IIPROCESSING DEFECT
Halyard EYE PACK convenience kit recalled for incorrect Betadine solution concentration
OTHERNationwide distribution
Halyard EYE PACK recalled for incorrect Betadine 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.
- Check if you have a Halyard EYE PACK (Model LVEY27) with lot number 1680076 or 1680590.
- Do not use the kit if you have one of the affected lots.
- Contact your supplier or AVID Medical for instructions on return or replacement.
Hazard
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Sold states
US Nationwide distribution in the state of California.
Affected count
260 kits
Manufactured in
9000 Westmont Dr, N/A, Toano, VA, United States
Products
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2763-2026More AVID Medical, Inc. recalls
- FDA-Device2026-07-29Halyard STANDARD LINE INSERTION PACK recalled for silicone seal defects causing fluid leakage risk
- FDA-Device2026-06-17Halyard Towel Six Pack recalled for non-sterilized sealed pouches
- FDA-Device2026-06-17Halyard Pain Pack Kit recalled for unsterilized pouches
- FDA-Device2026-06-17Halyard Drape Pack (Kit LMDP36-01) recalled for unsterilized pouches
- FDA-Device2026-06-17Halyard Eye Bag Pack recalled for non-sterilized sealed pouches
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