FDA Device recall Z-0719-2018
MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully pla…
- FDA Device
- Class II
- terminated
- Published 2018-03-07
On 2018-03-07 the FDA classified a Class II recall of MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully pla… by Medistim Asa, citing A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0719-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-04-25 |
| Published | 2018-03-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medistim Asa |
| Distribution | NY |
Product
MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.
Reason
A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening.
Identifiers
| code_info | UDI: 7070554101198 Serial#: 1170 and 1294 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0719-2018%22
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