Recall Z-1480-2013— Kreg Medical Inc.

Name: FDA recall Z-1480-2013
Creator: U.S. Food and Drug Administration
Published: 2012-08-02

Class II · Terminated

Class II FDA medical device recall by Kreg Medical Inc., initiated 2012-08-02, terminated 2018-03-02. FDA's recall record names no specific 510(k) clearance for this event. Product: E-Z WIDER BARIATRIC CHAIR BED; Single Motion Expandable Width Technology. Reason: An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during patient use, leaving the patient in a forward tilt position..

Recalling firm: Kreg Medical Inc.
Classification: Class II
Status: Terminated
Initiated: 2012-08-02
Terminated: 2018-03-02
Firm location: Chicago, IL, United States

Product description

E-Z WIDER BARIATRIC CHAIR BED; Single Motion Expandable Width Technology

Reason for recall

An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during patient use, leaving the patient in a forward tilt position.

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