Ferno Model 35X PROFlexx Stretchers, one unit per package

FDA device recall Z-0995-2015 · posted 2015-01-16 · Terminated

Recall details

Recalling firm

Ferno-Washington Inc

Reason for recall

The wheel castor assemblies may be loosening on the stretchers.

Action taken

Ferno initiated contact with customers via email and telephone on Wednesday, December 3, 2014. The firm will replace all wheel caster assemblies.

Root cause

Mixed-up of materials/components

Status

Terminated

Product code

FPO

Quantity affected

46 units

Distribution

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

Date initiated

2014-12-03

Date posted

2015-01-16

Date terminated

2015-12-01

Location

Wilmington, OH