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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MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions. — Recall Details · AllClear