{"url_path":"/fda/device/recalls/Z-2656-2026","section_key":"summary","section_title":"DEVICE Recall: Bard Access Systems, Inc. — CK000495A\tPoly Midline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741121609    CK000566\tPoly Midline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741108051    CK000566\tPoly Midline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741108051      The Poly Per-Q-Cath Midline catheters are indicated for short or long term peripheral access to the peripheral…","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-2656-2026%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":214,"has_tables":false,"body_markdown":null}