Bard Access Systems, Inc. Recalls
15 recalls on record in the United States
Bard Access Systems, Inc. recalls CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Co
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialys
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Cod
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Co
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen U
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 0080
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 01108
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UD
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 011088540
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 0
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls 5605150 Power-Trialysis Short-Term Straight Dialysis Cathete
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. recalls BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK
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 obturator, due to it locking to the needle hub, due to out-of-tolerance dimensions and IFU unclarity, which may result in new needle placement, which may result in delayed therapy
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