{"url_path":"/fda/device/recalls/Z-2526-2026","section_key":"summary","section_title":"DEVICE Recall: PFM MEDICAL INC. — Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-21","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2526-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"PFM MEDICAL INC."},"word_count":104,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2526-2026\n\n**Recalling firm:** PFM MEDICAL INC.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-21\n**Report date:** 2026-07-01\n\n## Product\nMulti-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310\n\n## Reason\nA snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-cytotoxicity, which if in contact with a patient's vasculature could result in localized inflammation and tissue irritation.\n\n## Affected lots\nREF/UDI-DI/Lot(Expiration): 147305/04042301061829/1049868(10/14/2028); 147310/04042301033567/1049960(10/20/28)\n\n## Distribution\nUS Nationwide distribution in the states of NY, MD."}