FreshRecalls

Bard Access Systems recalls

14 recent recalls on record for Bard Access Systems in CPSC, NHTSA, and FDA data as of July 24, 2026 at 1:09 AM UTC.

Models with recalls

1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code (1)1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 3173108D PowerPICC (1)4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code (1)5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Co (1)5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code (1)5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen (1)7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code (1)CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code (1)CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code (1)CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code (1)CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code (1)CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code (1)CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code (1)OTP5000 THORA/PARA TRAY (1)

All Bard Access Systems recalls

FDA Class II · Medical device · July 8, 2026

4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2668-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2667-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2666-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2665-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2664-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2663-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2662-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2661-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Co recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2660-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 3173108D PowerPICC recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2659-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2658-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2657-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2656-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

OTP5000 THORA/PARA TRAY recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2655-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked July 24, 2026 at 1:09 AM UTC.