mo-Vis BVBA recalls
Every recall we track for mo-Vis BVBA — 7 in all, from 2023–2025 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
Recalls from mo-Vis BVBA peaked in 2025 (6); 7 since 2017. 29% rated “stop using now”.
All FDA recall records for mo-Vis BVBA since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 1 | 0 | 0 | 0 | 1 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 1 | 5 | 0 | 0 | 6 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled mo-Vis BVBA product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All mo-Vis BVBA recalls
2 shown- Stop using nowMedical device
mo-Vis BVBA recalls IDM-MICRO-R. Electrical wheelchair component.
mo-Vis recalls IDM-MICRO-R wheelchair components due to firmware issues causing unintended movement. Check serial numbers 1000-1690 for details.
mo-VisJul 10, 2025 - Stop using nowMedical device
mo-Vis BVBA recalls Scoot Control R-net, Product Number P015-61. The Scoot Control is intended to support a wheelchair attendant in
mo-Vis recalls Scoot Control R-net units due to throttle lever sticking, which may cause unwanted wheelchair movement and injury.
mo-VisNov 28, 2023
mo-Vis BVBA recall questions
How many recalls has mo-Vis BVBA had?
7 recalls from mo-Vis BVBA are on record with U.S. safety agencies, from 2023–2025.
What is the most recent mo-Vis BVBA recall?
mo-Vis BVBA recalls IDM-MICRO-R. Electrical wheelchair component., dated Jul 10, 2025. Every mo-Vis BVBA recall is listed on this page, newest first.
What should I do if I have a recalled mo-Vis BVBA product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new mo-Vis BVBA recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.