Bard Access Systems, Inc. Recalls

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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