{"url_path":"/fda/device/recalls/Z-2658-2026","section_key":"summary","section_title":"DEVICE Recall: Bard Access Systems, Inc. — CK000662\tPowerPICC SOLO HF Catheter 5 Fr Triple-Lumen\t  UDI-DI Code: 00801741129674      Catheter stylets provide internal reinforcement to aid in catheter placement.","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-2658-2026%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":154,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2658-2026\n\n**Recalling firm:** Bard Access Systems, Inc.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-21\n**Report date:** 2026-07-08\n\n## Product\nCK000662\tPowerPICC SOLO HF Catheter 5 Fr Triple-Lumen\t  UDI-DI Code: 00801741129674      Catheter stylets provide internal reinforcement to aid in catheter placement.\n\n## Reason\nDue to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.\n\n## Affected lots\nCK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741129674 Lot Number: REKT1554\n\n## Distribution\nWorldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY. The country of Belgium."}