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Argon Medical Devices, Inc recalls Scorpion Portal Vein Access Set - Product Usage: used to gain access to the hepatic vein and guide a sharp puncture tool
Recalled September 29, 2021 · FDA recall Z-2501-2021 · Argon Medical Devices
Hazard
As a result of design changes, sheaths have exhibited cracking/breaking at the tips. · FDA Class II
Units
20 units
Sold at
U.S. Nationwide distribution in the state of WA. O.U.S.: N/A
Description
As a result of design changes, sheaths have exhibited cracking/breaking at the tips.
Product
Scorpion Portal Vein Access Set - Product Usage: used to gain access to the hepatic vein and guide a sharp puncture tool (0.040 Stylet or 17ga Needle) through the parenchyma.
Manufacturer(s)
Argon Medical Devices, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →