Home / Recalls / Medical Devices
Permobil, Ab recalls Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II
Recalled October 11, 2017 · FDA recall Z-0005-2018 · Permobil, Ab
Hazard
There is a potential failure of the top plate assembly, which is the component that connects the seating system of the wheelchair to the base. · FDA Class II
Units
5539 units
Sold at
Nationwide and Australia, Benelux, Canada, Denmark, Finland, France, Germany, Israel, Norway, Sweden, and UAE
Description
There is a potential failure of the top plate assembly, which is the component that connects the seating system of the wheelchair to the base.
Product
Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
Manufacturer(s)
Permobil, Ab
Made in
Sweden
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →