FDA Class I · Medical device · September 23, 2026
DuoGlide Short-Term Straight Dialysis Catheter recall — Bard Access Systems, Inc.
this is a downstream recall of class I recall RES 98777
Official ID Z-2985-2026 · Official record ↗
Bard Access Systems recalls
17 recent recalls on record for Bard Access Systems in connected official government data as of October 22, 2026 at 6:00 PM 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)BD Needle Kit for Powered Driver 15mm x 15Ga (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)DuoGlide Short-Term Straight Dialysis Catheter (1)OTP5000 THORA/PARA TRAY (1)Power-Trialysis Short-Term Straight Dialysis Catheter (1)
All Bard Access Systems recalls
FDA Class I · Medical device · September 23, 2026
Power-Trialysis Short-Term Straight Dialysis Catheter recall — Bard Access Systems, Inc.
this is a downstream recall of class I recall RES 98777
Official ID Z-2984-2026 · Official record ↗
FDA Class I · Medical device · August 26, 2026
BD Needle Kit for Powered Driver 15mm x 15Ga recall — Bard Access Systems, Inc.
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 exp…
Official ID Z-2872-2026 · Official record ↗
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 ↗
Verify with the official sources:
- CPSC — consumer products ↗ (aggregated here)
- NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
Found something wrong or missing? Report a data error.
Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.