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mo-Vis BVBA recalls IDM-ARLITE-R. Electrical wheelchair component.
Recalled September 10, 2025 · FDA recall Z-2459-2025 · mo-Vis BVBA
Hazard
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. · FDA Class I
Units
25 units
Sold at
US Nationwide distribution in the state of TX.
Description
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
IDM-ARLITE-R. Electrical wheelchair component.
Manufacturer(s)
mo-Vis BVBA
Made in
Belgium
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →