mo-Vis BVBA: Device Recall
Recall #Z-2455-2025 · 07/10/2025
Class I: Dangerous
Recall Details
- Recall Number
- Z-2455-2025
- Classification
- Class I
- Product Type
- Device
- Recalling Firm
- mo-Vis BVBA
- Status
- Ongoing
- Date Initiated
- 07/10/2025
- Location
- Nevele, N/A, Belgium
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3 units
Reason for Recall
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
Product Description
Multi Joystick R-net. Electrical wheelchair component.
Distribution Pattern
US Nationwide distribution in the state of TX.
Other Recalls by mo-Vis BVBA
- Class I: Dangerous 07/10/2025
- Class I: Dangerous 07/10/2025
- Class I: Dangerous 07/10/2025
- Class I: Dangerous 07/10/2025
- Class I: Dangerous 07/10/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.