{"url_path":"/fda/device/recalls/Z-2657-2026","section_key":"summary","section_title":"DEVICE Recall: Bard Access Systems, Inc. — 5625240\tDuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen  UDI-DI Code: 00801741042119      The intended use of the Short-Term Dialysis Catheter is attaining temporary/short-term (less than 30 days) vascular access for hemodialysis, hemoperfusion, or apheresis therapy via the jugular, subclavian, or femoral vein.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-21","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2657-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Bard Access Systems, Inc."},"word_count":176,"has_tables":false,"body_markdown":null}