Recall database

Dilator, Vessel, For Percutaneous Catheterization recalls

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

Showing 1–2 of 2 recalls

Class IOngoingZ-2705-2026

Argon Medical Devices, Inc recalls One-Piece Introducer Tray

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

For Percutaneous Catheterization Vessel Dilator
Material/Component Contamination

Argon Medical Devices,…TXJul 22, 2026

Class IIOngoingZ-1732-2025

Galt Medical Corporation recalls B Braun Interventional Coaxial Dilator REF: KIT-018-47

Due to a potential open seal in the sterile barrier packaging .

For Percutaneous Catheterization Vessel Dilator
Process control

Galt Medical Corporati…TXMay 14, 2025