Official recall notice
FDA DeviceClass IINotable
FDA Recall: Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
- Recall date
- 2026-08-05
- Brand
- Permobil Inc
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
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,
Product description
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,
Affected products
All Units operating with firmware version 1.26.2/UDI:(01)17330818345674