Recall Z-0995-2015— Ferno-Washington Inc
Class II · Terminated
Class II FDA medical device recall by Ferno-Washington Inc, initiated 2014-12-03, terminated 2015-12-01. FDA's recall record names no specific 510(k) clearance for this event. Product: Ferno Model 35X PROFlexx Stretchers, one unit per package. Reason: The wheel castor assemblies may be loosening on the stretchers..
- Recalling firm
- Ferno-Washington Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-12-03
- Terminated
- 2015-12-01
- Firm location
- Wilmington, OH, United States
Product description
Ferno Model 35X PROFlexx Stretchers, one unit per package
Reason for recall
The wheel castor assemblies may be loosening on the stretchers.
Data sourced from openFDA. This site is unofficial and independent of the FDA.