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

FDA Recall #Z-2458-2025 — Class I — July 10, 2025

Recall #Z-2458-2025 Date: July 10, 2025 Classification: Class I Status: Ongoing

Product Description

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

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.

Recalling Firm

mo-Vis BVBA — Nevele, N/A

Classification

Class I — Reasonable probability of serious adverse health consequences or death.

Product Type

Devices

Product Quantity

3 units

Distribution

US Nationwide distribution in the state of TX.

Code Information

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

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medical device immediately and consult your healthcare provider. Contact the recalling firm for instructions on return or replacement. If you experienced an adverse event, inform your doctor.

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