Recall Z-2826-2015— Ferno-Washington Inc

Name: FDA recall Z-2826-2015
Creator: U.S. Food and Drug Administration
Published: 2015-08-03

Class II · Terminated

Class II FDA medical device recall by Ferno-Washington Inc, initiated 2015-08-03, terminated 2016-01-20. FDA's recall record names no specific 510(k) clearance for this event. Product: Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital patient transport.. Reason: Hole elongation in the telescoping load frame channel. A hole elongation could affect the ability of the retention pin to stay seated which is necessary to preclude movement of the telescoping load frame..

Recalling firm: Ferno-Washington Inc
Classification: Class II
Status: Terminated
Initiated: 2015-08-03
Terminated: 2016-01-20
Firm location: Wilmington, OH, United States

Product description

Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital patient transport.

Reason for recall

Hole elongation in the telescoping load frame channel. A hole elongation could affect the ability of the retention pin to stay seated which is necessary to preclude movement of the telescoping load frame.

Data sourced from openFDA. This site is unofficial and independent of the FDA.