{"url_path":"/fda/device/recalls/Z-3114-2026","section_key":"summary","section_title":"DEVICE Recall: C.R. Bard Inc — Products that contain the Pericare Wipes:    Bardex Lubricath Foley Catheter Tray  REF:  899914  899916  899918  UDI codes:  00801741024801¿\t10801741024808  00801741024818¿\t10801741024815  00801741024825¿\t10801741024822    SureStep\" Foley Tray System with Bardex¿ Lubricath Temp Sensing Foley Catheter  REF: A119416M  UDI code: 00801741073700\t10801741073707  \t  SureSt…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-06-25","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3114-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"C.R. Bard Inc"},"word_count":656,"has_tables":false,"body_markdown":null}