Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MEDISTIM VERIQ SYSTEM Recalled by Medistim Asa Due to A system component overheated causing melting of the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medistim Asa directly.
Affected Products
MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.
Quantity: 2
Why Was This Recalled?
A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening.
Where Was This Sold?
Distributed to New York.
About Medistim Asa
Medistim Asa has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report