Class II — Medistim Asa
| Recalling firm | Medistim ASA |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening. |
| Product | MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions. |
| Quantity | 2 |
| Distribution | Distributed to New York. |
| Initiated | 2017-04-25 |
| Classified | 2018-02-26 |
| Terminated | 2024-05-03 |
| Recall number | Z-0719-2018 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Medistim Asa (Z-0719-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/78973/
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