mo-Vis BVBA: Device Recall

Recall #Z-2457-2025 · 07/10/2025

Class I: Dangerous

Recall Details

Recall Number
Z-2457-2025
Classification
Class I
Product Type
Device
Recalling Firm
mo-Vis BVBA
Status
Ongoing
Date Initiated
07/10/2025
Location
Nevele, N/A, Belgium
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
15 units

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.

Product Description

IDM-MULTI-R. Electrical wheelchair component.

Distribution Pattern

US Nationwide distribution in the state of TX.

Other Recalls by mo-Vis BVBA

View all recalls by mo-Vis BVBA →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.