Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031 — Class II medical device recall Z-2795-2026
Ongoing recall by Permobil Inc, reported 2026-08-05, distributed nationwide. This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to mainta
| Recall number | Z-2795-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Permobil Inc, Lebanon, TN, United States |
| Recall initiated | 2024-02-29 |
| Classified | 2026-07-24 |
| Reported by FDA | 2026-08-05 |
| Distributed | Nationwide (US) |
| Quantity | 140 units |
| Reason classes | specification failure, software |
| UPC / GTIN / UDI-DI | 17330818345674 |
| Model numbers | 120031 |
Product
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
Reason for recall
This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall from the wheelchair or the wheelchair to tip over,
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-2795-2026. 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.