FDA Device recall Z-2795-2026
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
- FDA Device
- Class II
- ongoing
- Published 2026-08-05
On 2026-08-05 the FDA classified a Class II recall of Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3 by Permobil, citing 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 us….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2795-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-02-29 |
| Published | 2026-08-05 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Permobil |
| Distribution | US |
Product
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
Reason
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,
Identifiers
| code_info | All Units operating with firmware version 1.26.2/UDI:(01)17330818345674 |
|---|
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-2795-2026%22
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