Ferno Model 35X PROFlexx Stretchers, one unit per package
FDA Recall Z-0995-2015 · Posted 2015-01-16
Recalling FirmFerno-Washington Inc
Recall StatusTerminated
Product CodeFPO
Date Initiated2014-12-03
Date Terminated2015-12-01
Product Quantity46 units
Reason for Recall
The wheel castor assemblies may be loosening on the stretchers.
Firm Action
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
Distribution Pattern
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.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.