{"url_path":"/fda/device/recalls/Z-2305-2026","section_key":"summary","section_title":"DEVICE Recall: DeRoyal Industries Inc — DeRoyal Industries Inc.   Ref 46-406, Covaderm Plus, Vascular Access Dressing 6\"x6\" (15cmx15cm)","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-18","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2305-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"DeRoyal Industries Inc"},"word_count":64,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2305-2026\n\n**Recalling firm:** DeRoyal Industries Inc\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-18\n**Report date:** 2026-06-10\n\n## Product\nDeRoyal Industries Inc.   Ref 46-406, Covaderm Plus, Vascular Access Dressing 6\"x6\" (15cmx15cm)\n\n## Reason\nSterile wound dressing, lacks  sterility assurance\n\n## Affected lots\nLot: 63295141/UDI: None\n\n## Distribution\nUS Nationwide distribution in the states of FL & NC."}