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Argon Medical Devices, Inc recalls General Biospy Tray, REF: GUTS1000
Recalled July 22, 2026 · FDA recall Z-2706-2026 · Argon Medical Devices
Hazard
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. · FDA Class I
Units
1800
Sold at
Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.
Description
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Product
General Biospy Tray, REF: GUTS1000
Manufacturer(s)
Argon Medical Devices, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →