Permobil, Ab recalls Permobil powered wheelchairs, Model Numbers: (a) M300 PS, (b) C300 PS, (c) C350 PS, (d) C500 PS, (e) C400 PS Product Us…

Recall date

August 15, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-3178-2018

FDA classification

Class II

Brand / firm

Permobil, Ab

Sold / distributed

Worldwide Distribution - US Nationwide

Why it was recalled

This correction decision has been made because of a potential failure of one or both backrest bars providing back support. If one or both back support telescoping bars fail the user could fall back leading to a potential injury.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Permobil 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.