FDA-Device2026-07-29Class IIPROCESSING DEFECT
Halyard EYE PACK convenience kit recalled for incorrect Betadine solution concentration
What this means
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.
The agency's original wording
Hazard
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Intended for
Adults
Illnesses reported
None reported
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 recalls
- FDA-Device2026-09-09AVID Medical neurological surgical kits recalled for endotoxin variability in sponges
- FDA-Device2026-09-09Halyard medical convenience kits recalled for neurological sponges with inconsistent endotoxin levels
- FDA-Device2026-09-09Halyard medical surgical kits recalled for neurological sponges with variable endotoxin levels
- FDA-Device2026-07-29Halyard STANDARD LINE INSERTION PACK recalled for silicone seal defects causing fluid leakage risk
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