Mo-Vis BVBA recalls IDM-MULTI-R. Electrical wheelchair component.

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.

IDM-MULTI-R. Electrical wheelchair component.

An URGENT: MEDICAL DEVICE RECALL R-NET JOYSTICKS notification dated 07/10/2025 was sent to consignees instructing them to upgrade affected devices according to the provided Annex 2 or by emailing contact@mo-vis.com to coordinate return. The software upgrade of affected devices should be conducted during the next scheduled annual maintenance of the joystick. These actions should be verified. Questions can be directed via email to contact@mo-vis.com or by phone at +32 9 335 28 60.

• FDA enforcement recordOfficial FDA database entry for Z-2457-2025
• FDA device classification · KNNOfficial FDA classification for this device type
• CFR regulation · 21 CFR 890.3920The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find mo-Vis BVBASearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.