All-round Joystick R-net Light. Electrical wheelchair… recallZ-2458-2025 · mo-Vis BVBA · initiated Jul 10, 2025
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from mo-Vis BVBA or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
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.
FDA root cause category: Device Design
What the company is doing
An URGENT: MEDICAL DEVICE RECALL R-NET JOYSTICKS notification dated 07/10/2025 was sent to consignees instructing them to upgrade affected devices according to the provided Annex 2 or by emailing [email protected] to coordinate return. The software upgrade of affected devices should be conducted during the next scheduled annual maintenance of the joystick. These actions should be verified. Questions can be directed via email to [email protected] or by phone at +32 9 335 28 60.
Recall details
- Recall number
- Z-2458-2025
- Status
- Open, Classified
- Initiated by the company
- Jul 10, 2025
- Posted by the FDA
- Sep 2, 2025
- Recalling firm
- mo-Vis BVBA
- Quantity
- 3 units
- Product code
- KNN
- Distribution
- US Nationwide distribution in the state of TX.
Product description
All-round Joystick R-net Light. Electrical wheelchair component.
Code information (models, lots, serial numbers)
Model No. P002-76; UDI-DI: 05407008320096; Serial No. 1000 to 2647.
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- mo-Vis P002-76mo-Vis · Components, Wheelchair1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 97354).
- Z-2454-2025 · Open, ClassifiedMicro Joystick R-net. Electrical wheelchair component.
- Z-2455-2025 · Open, ClassifiedMulti Joystick R-net. Electrical wheelchair component.
- Z-2456-2025 · Open, ClassifiedIDM-MICRO-R. Electrical wheelchair component.
- Z-2457-2025 · Open, ClassifiedIDM-MULTI-R. Electrical wheelchair component.
- Z-2459-2025 · Open, ClassifiedIDM-ARLITE-R. Electrical wheelchair component.
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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