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Medical Device

General Biospy Tray, REF: GUTS1000

Recall date: 2026-07-22 · Source: FDA_DEVICE
Brand / Firm
Argon Medical Devices, Inc
Product
General Biospy Tray, REF: GUTS1000
Reason for recall
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Units affected
1800
Description
General Biospy Tray, REF: GUTS1000
View official recall notice →