Notice names this product. AVID Medical’s Halyard EYE PACK is named in FDA Class II recall Z-2763-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Incorrect concentration of Betadine solution contained within certain AVID convenience kits. Identifying details: Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027).. Units affected: 260 kits. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Company / brand: AVID Medical
Affected product: Halyard EYE PACK
Official ID Z-2763-2026 · Official record ↗
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Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.