Recall database

Bard Access Systems, Inc. recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 13–15 of 15 recalls

Class IIOngoingZ-2656-2026

Bard Access Systems, Inc. recalls CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000…

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

Bard Access Systems, I…UTJul 8, 2026

Class IIOngoingZ-2655-2026

Bard Access Systems, Inc. recalls OTP5000 THORA/PARA TRAY

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

Bard Access Systems, I…UTJul 8, 2026

Class IOngoingZ-1507-2025

Bard Access Systems, Inc. recalls BD 4 Fr Single-Lumen PowerPICC Catheters

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 i…

Bard Access Systems, I…UTApr 23, 2025