FDAApril 25, 2017device
MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening.
What to do
FDA enforcement status: Terminated
Brands named
medistim asamedistim
UPCs
7070554101198
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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