Multi Joystick wheelchair controls recalled over unintended movement at power-up
Multi Joystick R-net wheelchair controls with firmware 2.3 or lower are recalled because timing variations may skip the neutral check, producing unintended movement on power-up. 3 units are affected.
The agency’s classification
FDA (Devices): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 5/5 (Critical).
Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The rubric assigns 5 to any FDA Class I recall, and the FDA classified this wheelchair joystick action as Class I.
Plain-English summary
The Multi Joystick R-net, an electrical wheelchair component, model P002-62, UDI-DI 05407008320041, is being recalled for serial numbers 1000 to 1690. The recall covers 3 units distributed in Texas.
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. The FDA classified the action as Class I, its most serious category.
Wheelchair users and providers should check the model and serial number against the recall notice and follow the manufacturer's instructions for a firmware update or replacement.
The recalled product
- Product
- Multi Joystick R-net. Electrical wheelchair component.
- Manufacturer
- mo-Vis BVBA
- Category
- Medical Device — Mobility Device
- Affected units
- 3
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Model No. P002-62
- UDI-DI: 05407008320041
- Serial No. 1000 to 1690.
Distribution
Part of a larger recall action
This product is one of 6 recalled by mo-Vis BVBA under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 6 products in this recall →Related recalls
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