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Bard Access Systems, Inc. Recalls

Overview of recall records associated with Bard Access Systems, Inc., including dates, categories and classifications where available.

14recall records

Jul 8, 2026latest record date

Jul 8, 2026earliest record date

Recall history in this database

Classification mix: Class II: 14.

Medical DeviceJul 8, 2026

Bard Access Systems CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code recall — FDA Z-2656-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter recall — FDA Z-2661-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code recall — FDA Z-2662-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code recall — FDA Z-2667-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen recall — FDA Z-2657-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code recall — FDA Z-2664-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 recall — FDA Z-2659-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code recall — FDA Z-2658-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 recall — FDA Z-2655-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code recall — FDA Z-2665-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code recall — FDA Z-2663-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A recall — FDA Z-2668-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 recall — FDA Z-2666-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Medical DeviceJul 8, 2026

Bard Access Systems 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr recall — FDA Z-2660-2026

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

Class IIFDA: OngoingBard Access Systems, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Bard Access Systems, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.