Recall database

Gauze/Sponge, Internal, X-Ray Detectable recalls

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

Showing 1–1 of 1 recalls

Class IOngoingZ-2708-2026

Argon Medical Devices, Inc recalls Arterial Line Kit 20ga x 6

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

X-Ray Detectable Internal Gauze/Sponge
Material/Component Contamination

Argon Medical Devices,…TXJul 22, 2026