Ferno-Washington Inc recalls Ferno Model 35X PROFlexx Stretchers, one unit per package

Recall date

December 3, 2014

Source

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

Recall number

Z-0995-2015

FDA classification

Class II

Brand / firm

Ferno-Washington Inc

Sold / distributed

The affected product was distributed to the following states: OH, MA, HI, NJ, TN, TX, MO, and GA. The affected product was distributed to the following foreign countries: Canada, Germany and Venezuela.

Why it was recalled

The wheel castor assemblies may be loosening on the stretchers.

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

What was recalled

Ferno Model 35X PROFlexx Stretchers, one unit per package