mo-Vis BVBA recalls All-round Joystick R-net Light. Electrical wheelchair component.

Recall date

July 10, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2458-2025

FDA classification

Class I

Brand / firm

mo-Vis BVBA

Sold / distributed

US Nationwide distribution in the state of TX.

Why it was recalled

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.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

All-round Joystick R-net Light. Electrical wheelchair component.