Reported Sep 10, 2025 · Ongoing

IDM-MULTI-R. Electrical wheelchair component.

mo-Vis BVBA

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: mo-Vis BVBA · Biebuyckstraat 15D · Nevele, N/A · N/A

Is this the product you have?

  • IDM-MULTI-R. Electrical wheelchair component.
Lot codes and dates
  • Model No. PRSPS0016
  • UDI-DI
    • 05407008320850
    • Serial No. 1000 to 1690
Amount recalled
15 units

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

  • Nationwide
  • TX

Why it was recalled

Stop using this product now

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.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:41 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.