Wheelchair component Recall: mo-Vis IDM-MICRO-R
Announced 2025-09-10 · FDA
The recall covers the IDM-MICRO-R electrical wheelchair component from mo-Vis. Firmware versions 2.3 and lower may cause timing variations between software tasks, potentially skipping the neutral check and causing unintended movement on power-up when the joystick is out of neutral. Three units were distributed nationwide in the United States, with distribution in Texas; recall numbers include Model No. P002-62, UDI-DI 05407008320041, and Serial No 1000-1690.
| Brand | mo-Vis BVBA |
|---|---|
| Product | Multi Joystick R-net. Electrical wheelchair component. |
| Reason | 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. |
| Severity | critical |
| Units affected | 15 |
| Distribution | US Nationwide distribution in the state of TX. |
| Agency | FDA |
| Recall / campaign no. | Model No. P002-62; UDI-DI: 05407008320041; Serial No. 1000 to 1690. |
WHAT YOU SHOULD DO
- Stop using the component and disconnect power until told otherwise.
- Contact mo-Vis or your wheelchair supplier for recall instructions and potential replacement.
- Have your device's model (P002-62), firmware version (2.3 or lower), and serial number (1000–1690) ready for verification.
- Do not attempt to modify firmware; await guidance from the manufacturer or FDA.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.