Oslo, N/A, Norway
Medistim Asa recalls
2 recalls recorded since 2018, most recently on 26 September 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)1
Terminated or completed1
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 26 September 2025
- Reason
- Printer Support Module (PSM) may be subject to insufficient soldering, which may cause loosening of the wires and system to shut down. Affected devices need to have their Printer Support Modules replaced.
- Distribution
- Domestic distribution to CO, MI, MN, TN, TX. International distribution to Australia, Austria, Germany, Finland, India, Japan, Russia, China, Saudi Arabia.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0410-2026
- Brand Name: Medistim MiraQ System Product Name: Medistim MiraQ System Model/Catalog Number: MQC04001, MQC14001, MQU14011, MQV12011 Software Version: Not applicable Product Description: Ultrasound device for intraoper
Terminated Class II Medical devices
- Recall started
- 25 April 2017
- Terminated
- 3 May 2024
- Reason
- A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening.
- Distribution
- Distributed to New York.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0719-2018
- MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.