{"url_path":"/fda/device/recalls/Z-2667-2026","section_key":"summary","section_title":"DEVICE Recall: Bard Access Systems, Inc. — CK000880\tProvena Midline Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741188770    S4153108BDP\tProvena Midline Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741154003    S4153108BP\tProvena Midline Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741153990    S4153108D\tProvena Midline Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741153952    S4153108DCP\tProv…","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-2667-2026%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":447,"has_tables":false,"body_markdown":null}