General Biospy Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IOngoing
Summary: Argon Medical Devices, Inc is recalling General Biospy Tray, REF: GUTS1000. Reason: Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
What is being recalled
General Biospy Tray, REF: GUTS1000
Why
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
How serious is it
Class I is the most serious level: FDA considers there is a reasonable probability that using or being exposed to this product will cause serious health problems or death.
Where it was sold
Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago. (states named: Puerto Rico)
How to tell if yours is affected
REF/UDI-DI Box:Unit/Lot(Expiration): GUTS1000/20886333001594:00886333001590/11649760(3/31/2028)
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2706-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class I |
| Status | Ongoing |
| Recall started | June 1, 2026 |
| Reported | July 22, 2026 |
| Company | Argon Medical Devices, Inc |
| Company location | Athens, TX, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 1800 |
More recalls from Argon Medical Devices, Inc · all medical device recalls · recalls from June 2026