MEDISTIM VERIQ SYSTEM — Class II medical device recall Z-0719-2018
Terminated recall by Medistim Asa, reported 2018-03-07, distributed in NY. A system component overheated causing melting of the connector and emission of smoke through the systems louds
| Recall number | Z-0719-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medistim Asa, Oslo, N/A, Norway |
| Recall initiated | 2017-04-25 |
| Classified | 2018-02-26 |
| Reported by FDA | 2018-03-07 |
| Terminated | 2024-05-03 |
| Distributed | NY |
| Quantity | 2 |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 07070554101198 |
| Serial numbers | 1170, 1294 |
| Model numbers | VQ4122 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0719-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.