FDA recall Z-0006-2018

Permobil, Ab · Class II · device

Product

Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500

Reason for recall

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.

Distribution

Nationwide and Australia, Benelux, Canada, Denmark, Finland, France, Germany, Israel, Norway, Sweden, and UAE

Key facts

Status
Terminated
Initiation date
2017-09-01
Report date
2017-10-11
Termination date
2021-05-04
Voluntary/Mandated
Voluntary: Firm initiated
Location
Timra, N/A, Sweden

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0006-2018