mo-Vis BVBA
mo-Vis BVBA appears in FDA public data with 7 recalls — including 6 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2456-2025, Class I) was initiated on July 10, 2025.
Summary
- Total Recalls
- 7 (6 Class I)
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2456-2025 | Class I | IDM-MICRO-R. Electrical wheelchair component. | July 10, 2025 |
| Z-2454-2025 | Class I | Micro Joystick R-net. Electrical wheelchair component. | July 10, 2025 |
| Z-2459-2025 | Class I | IDM-ARLITE-R. Electrical wheelchair component. | July 10, 2025 |
| Z-2455-2025 | Class I | Multi Joystick R-net. Electrical wheelchair component. | July 10, 2025 |
| Z-2457-2025 | Class I | IDM-MULTI-R. Electrical wheelchair component. | July 10, 2025 |
| Z-2458-2025 | Class I | All-round Joystick R-net Light. Electrical wheelchair component. | July 10, 2025 |
| Z-0713-2024 | Class II | Scoot Control R-net, Product Number P015-61. The Scoot Control is intended to support a wheelchair a | November 28, 2023 |