{"url_path":"/fda/device/recalls/Z-2763-2026","section_key":"summary","section_title":"DEVICE Recall: AVID Medical, Inc. — Halyard EYE PACK. Model/Catalog Number: LVEY27    Convenience kit.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-07","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2763-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"AVID Medical, Inc."},"word_count":73,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2763-2026\n\n**Recalling firm:** AVID Medical, Inc.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-07\n**Report date:** 2026-07-29\n\n## Product\nHalyard EYE PACK. Model/Catalog Number: LVEY27    Convenience kit.\n\n## Reason\nIncorrect concentration of Betadine solution contained within certain AVID convenience kits.\n\n## Affected lots\nModel/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027).\n\n## Distribution\nUS Nationwide distribution in the state of California."}