Bard Access Systems, Inc.
15 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Bard Access Systems, Inc. and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-07-08FDA-DeviceClass IIBard Access Systems biopsy trays recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard Provena Midline Catheters recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard PowerPICC catheters recalled for lidocaine quality issue
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard Groshong NXT catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard PowerPICC Provena catheters recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard PowerMidline Catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard PowerMidline Catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard Power-Trialysis dialysis catheters recalled for lidocaine defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard Power-Trialysis dialysis catheters recalled for lidocaine defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard PowerPICC SV catheters recalled for lidocaine defects
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard PowerPICC SOLO HF Catheter recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard DuoGlide dialysis catheter recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard Poly Midline Catheter recalled for lidocaine manufacturing defects
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceClass IIBard Access Systems drainage trays recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2025-04-23FDA-DeviceClass IBD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196, 9174118, CK000955, 3174135, CK000617, CK000839, 3194355, 6174118, 3194135, 3194335, 2174108, 9194118, 3194118, 1174118, CK000285C, CK000335A, CK000796, 1194108D, CK000757, CK001042, 9174108, 1174108D1, CK000631B, 3194155, 3174108, CK000567, 1194108D4, 1174108D2, CK000677, CK000864, CK000937A, CK000930, CK001027, 1174108D, CK000867, CK000900, CK000315A, CK000589A, CK000854B, CK000897,
Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfort, phlebitis, bleeding, air embolism, foreign body embolism, infection and interruption to therapy.
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