mo-Vis BVBA 2025-09-10 Health critical FDA
Health · FDA · Recall #FDA-Z-2456-2025
IDM-MICRO-R. Electrical wheelchair component. Recall
Issued September 10, 2025 · mo-Vis BVBA
In September 2025, mo-Vis BVBA recalled the IDM-MICRO-R. Electrical wheelchair component., a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using IDM-MICRO-R. Electrical wheelchair component. right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact mo-Vis BVBA to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- mo-Vis BVBA
- Category
- Health
- Recall date
- September 10, 2025
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the state of TX.
- Recall number
- FDA-Z-2456-2025
- Made in
- Belgium
- Issuing agency
- FDA
In context
- mo-Vis BVBA has 2 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.