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Medistim Asa recalls MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeo
Recalled March 7, 2018 · FDA recall Z-0719-2018 · Medistim Asa
Hazard
A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening. · FDA Class II
Units
2
Sold at
Distributed to New York.
Description
A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening.
Product
MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.
Manufacturer(s)
Medistim Asa
Made in
Norway
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →