FDA recall record · openFDA

mo-Vis BVBA

7 FDA recalls on record (2023–2025) — 7 device. 7 still ongoing.

Class I (most serious)

Class II

Class III

ongoing

How to read this. A recall count is not a quality verdict — large manufacturers recall more simply by volume, and a voluntary recall is the safety system working as intended. The signal to weight is the Class I count (the FDA's most-serious tier — reasonable probability of serious harm or death) and whether recalls are still ongoing. Most recalls are Class II/III. "Ongoing" reflects openFDA's last-published status — device recalls often stay marked ongoing long after they're resolved in practice; confirm current status at the FDA.

Most common reasons

Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result 6

In rare cases, the lever of the throttle can get temporarily stuck during the movement and does not come back to its neu 1

Recalls

IDM-MICRO-R. Electrical wheelchair component. Class I 2025-07-10 Micro Joystick R-net. Electrical wheelchair component. Class I 2025-07-10 IDM-ARLITE-R. Electrical wheelchair component. Class I 2025-07-10 All-round Joystick R-net Light. Electrical wheelchair component. Class I 2025-07-10 IDM-MULTI-R. Electrical wheelchair component. Class I 2025-07-10 Multi Joystick R-net. Electrical wheelchair component. Class I 2025-07-10 Scoot Control R-net, Product Number P015-61. The Scoot Control is intended to support a wheelchair attendant in controll Class II 2023-11-28

RECORDED — these are the FDA's published recall enforcement records (openFDA). Recalls are listed under the exact firm name as filed; a large manufacturer may also file under name variants, so this may not be the company's complete cross-variant record — confirm at the FDA recall database. This page informs and routes; it is not medical advice or a verdict on the company.

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