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FDA · Medical devicesClass I

mo-Vis BVBA medical device recall: Micro Joystick R-net. Electrical wheelchair component

Software problems

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Medical devices
Classification
Class I
Status
Ongoing
Event ID
97354
Recall initiated
Jul 10, 2025
Classified by FDA
Sep 2, 2025
Posted in Enforcement Report
Sep 10, 2025
Recalling firm
mo-Vis BVBA
Firm location
Nevele, Belgium
Initiated by
Voluntary: Firm initiated
Firm notified customers by
E-Mail
Products in this event
6

What to do

Compare the product, lot or serial numbers below with what you have. If you use a prescription drug or medical device in this recall, talk to your pharmacist or health care provider before you stop using it, and follow the firm's instructions.

View the official FDA record ↗

Reason for recall

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 the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Jul 10, 2025. FDA classified it 54 days later, on Sep 2, 2025. This recall event covers 6 separate products, each with its own FDA recall number. Distribution reported by FDA: US Nationwide distribution in the state of TX. mo-Vis BVBA has 2 recalls in our records.

Recalled products (6)

  • Z-2454-2025 Class I Ongoing

    Micro Joystick R-net. Electrical wheelchair component.

    Codes / lots: Model No. P002-52; UDI-DI: 05407008320027; Serial No. 1000 to 1690.

    Quantity: 3 units

  • Z-2455-2025 Class I Ongoing

    Multi Joystick R-net. Electrical wheelchair component.

    Codes / lots: Model No. P002-62; UDI-DI: 05407008320041; Serial No. 1000 to 1690.

    Quantity: 3 units

  • Z-2456-2025 Class I Ongoing

    IDM-MICRO-R. Electrical wheelchair component.

    Codes / lots: Model No. PRSPS0014; UDI-DI: 05407008320836; Serial No. 1000 to 1690.

    Quantity: 15 units

  • Z-2457-2025 Class I Ongoing

    IDM-MULTI-R. Electrical wheelchair component.

    Codes / lots: Model No. PRSPS0016; UDI-DI: 05407008320850; Serial No. 1000 to 1690.

    Quantity: 15 units

  • Z-2458-2025 Class I Ongoing

    All-round Joystick R-net Light. Electrical wheelchair component.

    Codes / lots: Model No. P002-76; UDI-DI: 05407008320096; Serial No. 1000 to 2647.

    Quantity: 3 units

  • Z-2459-2025 Class I Ongoing

    IDM-ARLITE-R. Electrical wheelchair component.

    Codes / lots: Model No. PRSPS00018. UDI-DI: 05407008320102; Serial No. 1000 to 2647.

    Quantity: 25 units

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA device enforcement dataset
Official notice
FDA Enforcement Report, event 97354
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.