Medical DeviceSep 23, 2026
Bard Access Systems Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150 recall — FDA Z-2984-2026
this is a downstream recall of class I recall RES 98777
Class IFDA: OngoingBard Access Systems, Inc.
Recall history in this database
Classification mix: Class II: 33, Class I: 5.
Medical DeviceSep 23, 2026
Bard Access Systems DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150 recall — FDA Z-2985-2026
this is a downstream recall of class I recall RES 98777
Class IFDA: OngoingBard Access Systems, Inc.
Medical DeviceAug 26, 2026
Bard Access Systems BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle recall — FDA Z-2872-2026
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 experience…
Class IFDA: OngoingBard Access Systems, Inc.
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.
Medical DeviceApr 23, 2025
Bard Access Systems BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540 recall — FDA Z-1507-2025
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…
Class IFDA: OngoingBard Access Systems, Inc.
Medical DeviceAug 3, 2022
Bard Access Systems Intraosseous needle and driver recall — FDA Z-1397-2022
BD Intraosseous Needle Kits may exhibit: 1) Increased force required to remove the stylet from intraosseous needle during placement may cause removal of the entire needle assembly and loss…
Class IFDA: OngoingBard Access Systems, Inc.
Medical DeviceJul 7, 2021
Bard Access Systems 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm recall — FDA Z-1994-2021
Catheter convenience kits contain the incorrect guidewire. Kits were labeled with 70cm guidewires, but contained a 50cm guidewire.
Class IIFDA: TerminatedBard Access Systems Inc.
Medical DeviceMay 26, 2021
Bard Access Systems REF 7617400, Groshong NXT ClearVue Catheter, intermediate kit, 4F recall — FDA Z-1652-2021
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the…
Class IIFDA: TerminatedBard Access Systems Inc.
Medical DeviceMay 26, 2021
Bard Access Systems REF 7617405J, Groshong NXT ClearVue Catheter, Basic kit, 4F recall — FDA Z-1653-2021
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the…
Class IIFDA: TerminatedBard Access Systems Inc.
Medical DeviceMay 26, 2021
Bard Access Systems REF 9617408, Groshong NXT ClearVue Catheter with Sherlock Tip Location recall — FDA Z-1661-2021
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the…
Class IIFDA: TerminatedBard Access Systems Inc.
Medical DeviceMay 26, 2021
Bard Access Systems REF CK000379, Groshong NXT ClearVue Catheter with Sherlock Tip Location recall — FDA Z-1666-2021
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the…
Class IIFDA: TerminatedBard 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.