FDASeptember 1, 2017device
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
Official recall recorded by the U.S. Food & Drug Administration.
The 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.
What to do
FDA enforcement status: Terminated
Brands named
permobil abpermobilpermobil ab
UPCs
25370028592
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAPushTracker E2 component utilized with the SmartDrive MX2+ Power Assist Device (Part Numbers: MX2-32K, MX2-32P, MX2-32PK, MX2-33D, MX2-33P, MX2-33PK, MX2-33S, MX2-150, MX2-167, MX2-32D); a wearable watch that communicates with a SmartDrive Power Assist Device via the SmartDrive MX2+ Application2023-05-10
- FDAPushTracker E3 component utilized with the SmartDrive MX2+ Power Assist Device (Part Numbers: MX2-32K, MX2-32P, MX2-32PK, MX2-33D, MX2-33P, MX2-33PK, MX2-33S, MX2-150, MX2-167, MX2-32D); a wearable watch that communicates with a SmartDrive Power Assist Device via the SmartDrive MX2+ Application2023-05-10
- FDAPermobil powered wheelchairs, Model Numbers: (a) M300 PS, (b) C300 PS, (c) C350 PS, (d) C500 PS, (e) C400 PS Product Usage: The devices identified are intended to provide outdoor and indoor mobility to persons limited to a seated position that can operate a powered wheelchair.2018-08-15
- FDAElectric Wheelchair bases: a) C300 b) C350 c) C400 d) C5002017-09-01
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