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Argon Medical Devices, Inc recalls Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jugular or Femoral Deliver
Recalled August 2, 2023 · FDA recall Z-2239-2023 · Argon Medical Devices
Hazard
There is the potential that the vena Cava Filter may not perform as intended which may result in pulmonary embolism. · FDA Class II
Units
3.0
Sold at
US Nationwide distribution in the state of TX.
Description
There is the potential that the vena Cava Filter may not perform as intended which may result in pulmonary embolism.
Product
Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jugular or Femoral Delivery, STERILEO, RxOnly, CE 2797
Manufacturer(s)
Argon Medical Devices, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →