Nevele, N/A, Belgium
mo-Vis BVBA recalls
2 recalls recorded since 2018, most recently on 10 July 2025. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)2
Terminated or completed0
Class I (FDA)1
Ongoing Class I Medical devices
- Recall started
- 10 July 2025
- Reason
- 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.
- Distribution
- US Nationwide distribution in the state of TX.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-2456-2025, Z-2454-2025, Z-2459-2025, Z-2458-2025, Z-2457-2025, Z-2455-2025
- IDM-MICRO-R. Electrical wheelchair component.
- Micro Joystick R-net. Electrical wheelchair component.
- IDM-ARLITE-R. Electrical wheelchair component.
- All-round Joystick R-net Light. Electrical wheelchair component.
- IDM-MULTI-R. Electrical wheelchair component.
- Multi Joystick R-net. Electrical wheelchair component.
Ongoing Class II Medical devices
- Recall started
- 28 November 2023
- Reason
- In rare cases, the lever of the throttle can get temporarily stuck during the movement and does not come back to its neutral point by itself. If this happens during usage, an unwanted movement of the chair could be the result. An unwanted movement could result in damage to the wheelchair, material damage around the chair and/or injury to the user, attendant or by-standers.
- Distribution
- US States: TN, TX.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0713-2024
- Scoot Control R-net, Product Number P015-61. The Scoot Control is intended to support a wheelchair attendant in controlling or maneuvering a power chair
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.