Class IOngoingZ-2985-2026
Bard Access Systems, Inc. recalls DuoGlide Short-Term Straight Dialysis Catheter
this is a downstream recall of class I recall RES 98777
Bard Access Systems, I…UTSep 23, 2026
Bard Access Systems, Inc. recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–12 of 17 recalls
Class IOngoingZ-2984-2026
Bard Access Systems, Inc. recalls Power-Trialysis Short-Term Straight Dialysis Catheter
this is a downstream recall of class I recall RES 98777
Bard Access Systems, I…UTSep 23, 2026
Class IOngoingZ-2872-2026
Bard Access Systems, Inc. recalls BD Needle Kit for Powered Driver 15mm x 15Ga
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove o…
Bard Access Systems, I…UTAug 26, 2026
Class IIOngoingZ-2668-2026
Bard Access Systems, Inc. recalls 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT TISSU…
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems, I…UTJul 8, 2026
Class IIOngoingZ-2667-2026
Bard Access Systems, Inc. recalls CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 S4153…
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems, I…UTJul 8, 2026
Class IIOngoingZ-2666-2026
Bard Access Systems, Inc. recalls 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 1295108 Po…
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems, I…UTJul 8, 2026
Class IIOngoingZ-2665-2026
Bard Access Systems, Inc. recalls 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258…
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems, I…UTJul 8, 2026
Class IIOngoingZ-2664-2026
Bard Access Systems, Inc. recalls CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129…
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems, I…UTJul 8, 2026
Class IIOngoingZ-2663-2026
Bard Access Systems, Inc. recalls CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 P425410…
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems, I…UTJul 8, 2026
Class IIOngoingZ-2662-2026
Bard Access Systems, Inc. recalls CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 CK0007…
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems, I…UTJul 8, 2026
Class IIOngoingZ-2661-2026
Bard Access Systems, Inc. recalls 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lu…
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems, I…UTJul 8, 2026
Class IIOngoingZ-2660-2026
Bard Access Systems, Inc. recalls 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-D…
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems, I…UTJul 8, 2026