Official recall record
Scoot Control R-net, Product Number P015-61. The Scoot Control is intended to support a wheelchair attendant in controlling or maneuvering a
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-11-28
- Country of alert
- Belgium
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 05407008320119
- Brand on record
- mo-Vis BVBA
What the authority reported
In rare cases, the lever of the throttle can get temporarily stuck during the movement and does not come back to its neutral point by itself. If this happens during usage, an unwanted movement of the chair could be the result. An unwanted movement could result in damage to the wheelchair, material damage around the chair and/or injury to the user, attendant or by-standers.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2025-07-10 · US FDA — Medical Devices
IDM-MICRO-R. Electrical wheelchair component. - 2025-07-10 · US FDA — Medical Devices
Micro Joystick R-net. Electrical wheelchair component.
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