M5 Corpus Power Wheelchair REF — Class II medical device recall Z-2805-2026
Ongoing recall by Permobil Inc, reported 2026-08-05, distributed nationwide. This recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic.
| Recall number | Z-2805-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Permobil Inc, Lebanon, TN, United States |
| Recall initiated | 2025-06-19 |
| Classified | 2026-07-24 |
| Reported by FDA | 2026-08-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 715 wheelchairs |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 17330818334562 |
| Model numbers | 120032 |
Product
M5 Corpus Power Wheelchair REF,120032
Reason for recall
This recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive under restricted conditions, and may create an unstable condition in certain circumstances.
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-2805-2026. 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.