{"url_path":"/fda/device/recalls/Z-2007-2026","section_key":"summary","section_title":"DEVICE Recall: Medical Action Industries, Inc. 306 — Medical Action Industries Inc.   Pack Cath BHH,   REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-03-17","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2007-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Medical Action Industries, Inc. 306"},"word_count":96,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2007-2026\n\n**Recalling firm:** Medical Action Industries, Inc. 306\n**Classification:** Class I\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-03-17\n**Report date:** 2026-05-13\n\n## Product\nMedical Action Industries Inc.   Pack Cath BHH,   REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case\n\n## Reason\nConvenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold\"\n\n## Affected lots\nUDI:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789\n\n## Distribution\nUS distribution to state of: AZ OUS: None"}