Recall Z-2458-2025— mo-Vis BVBA
Class I · Ongoing
Class I FDA medical device recall by mo-Vis BVBA, initiated 2025-07-10. FDA's recall record names no specific 510(k) clearance for this event. Product: All-round Joystick R-net Light. Electrical wheelchair component.. 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..
- Recalling firm
- mo-Vis BVBA
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2025-07-10
- Firm location
- Nevele, N/A, Belgium
Product description
All-round Joystick R-net Light. Electrical wheelchair component.
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.