{"url_path":"/fda/device/recalls/Z-2409-2026","section_key":"summary","section_title":"DEVICE Recall: AVID Medical, Inc. — Halyard, Drape Pack. Kit Code: LMDP36-01.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-30","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2409-2026%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":68,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2409-2026\n\n**Recalling firm:** AVID Medical, Inc.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-30\n**Report date:** 2026-06-17\n\n## Product\nHalyard, Drape Pack. Kit Code: LMDP36-01.\n\n## Reason\nInadvertent distribution of sealed pouches that had not undergone validated sterilization.\n\n## Affected lots\nKit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/2028\n\n## Distribution\nUS Nationwide distribution in  the state of Iowa."}