# FDA recall Z-0719-2018

> **Medistim Asa** · Class II · device recall initiated 2017-04-25.

## 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.

## Distribution

Distributed to New York.

## Key facts

- **Recall number:** Z-0719-2018
- **Recalling firm:** Medistim Asa
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-04-25
- **Report date:** 2018-03-07
- **Termination date:** 2024-05-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Oslo, N/A, Norway

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0719-2018

## Citation

> AI Analytics. FDA recall Z-0719-2018. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-0719-2018. Source: US FDA. Licensed CC0.

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