IDM-ARLITE-R — Class I medical device recall Z-2459-2025
Ongoing recall by mo-Vis BVBA, reported 2025-09-10, distributed nationwide. Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which co
| Recall number | Z-2459-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | mo-Vis BVBA, Nevele, N/A, Belgium |
| Recall initiated | 2025-07-10 |
| Classified | 2025-09-02 |
| Reported by FDA | 2025-09-10 |
| Distributed | Nationwide (US) |
| Quantity | 25 units |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 05407008320102 |
| Serial numbers | 1000, 2647 |
| Model numbers | PRSPS00018 |
Product
IDM-ARLITE-R. Electrical wheelchair component.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2459-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.