FDA Device recall Z-2805-2026
M5 Corpus Power Wheelchair REF,120032
- FDA Device
- Class II
- ongoing
- Published 2026-08-05
On 2026-08-05 the FDA classified a Class II recall of M5 Corpus Power Wheelchair REF,120032 by Permobil, citing 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,….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2805-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-06-19 |
| Published | 2026-08-05 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Permobil |
| Distribution | US |
Product
M5 Corpus Power Wheelchair REF,120032
Reason
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.
Identifiers
| code_info | Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2805-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.