MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.
Reported: March 7, 2018 Initiated: April 25, 2017 #Z-0719-2018
Product Description
MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.
Reason for Recall
A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening.
Details
- Recalling Firm
- Medistim Asa
- Units Affected
- 2
- Distribution
- Distributed to New York.
- Location
- Oslo, N/A
Frequently Asked Questions
What product was recalled? ▼
MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.. Recalled by Medistim Asa. Units affected: 2.
Why was this product recalled? ▼
A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 7, 2018. Severity: Moderate. Recall number: Z-0719-2018.
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