FDAFDA · Food and drugs·Recall number Z-2456-2025
IDM-MICRO-R. Electrical wheelchair component.
Published September 10, 2025 · Recall initiated: July 10, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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 to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- mo-Vis BVBA
- Distributor
- US Nationwide distribution in the state of TX.
- Lot
- Model No. PRSPS0014; UDI-DI: 05407008320836; Serial No. 1000 to 1690.
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- Belgium
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