{"url_path":"/fda/device/recalls/Z-2664-2026","section_key":"summary","section_title":"DEVICE Recall: Bard Access Systems, Inc. — CK000525B\tPowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741236129    CK000883\tPowerPICC Provena Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741188800    CK000884A\tPowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741219177    CK001000\tPowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741223020    CK0…","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-2664-2026%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":782,"has_tables":false,"body_markdown":null}