Bard Access Systems, Inc. recalls
17 recalls.
- DuoGlide Short-Term Straight Dialysis Catheter recall (Bard Access Systems, Inc.)
Medical deviceClass IReported September 23, 2026 · this is a downstream recall of class I recall RES 98777 - Power-Trialysis Short-Term Straight Dialysis Catheter recall (Bard Access Systems, Inc.)
Medical deviceClass IReported September 23, 2026 · this is a downstream recall of class I recall RES 98777 - BD Needle Kit for Powered Driver 15mm x 15Ga recall (Bard Access Systems, Inc.)
Medical deviceClass IReported August 26, 2026 · After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary... - 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code:... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - OTP5000 THORA/PARA TRAY recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by...