Wheelchair Joystick Recalled for Unintended Movement on Power-Up
The FDA is recalling 3 Multi Joystick R-net electrical wheelchair components due to a firmware defect that may cause unintended wheelchair movement when powered on. Firmware versions 2.3 and lower are affected.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: FDA Class I classification indicates the highest level of regulatory concern. The firmware defect poses a risk of serious injury due to unintended wheelchair movement at power-up. No illnesses or injuries have been reported.
Plain-English summary
The FDA is recalling the Multi Joystick R-net electrical wheelchair component manufactured by mo-Vis BVBA. The affected devices are Model No. P002-62 with serial numbers 1000 to 1690 and UDI-DI 05407008320041.
Devices with firmware versions 2.3 and lower contain a timing defect in the software that may cause the wheelchair to skip its neutral position check during power-up. This can result in unintended wheelchair movement when the joystick is not in the neutral position.
Three units have been distributed in Texas. Users of affected devices should contact mo-Vis BVBA regarding this firmware issue and any necessary corrective actions.
The recalled product
- Product
- Multi Joystick R-net. Electrical wheelchair component.
- Manufacturer
- mo-Vis BVBA
- Hazard
- unintended-movement
- firmware-defect
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
Distributed nationwide across the United States.
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