Recall Z-0522-2014— mobility unlimited inc

Class II · Terminated

Class II FDA medical device recall by mobility unlimited inc, initiated 2013-04-11, terminated 2014-10-08. FDA's recall record names no specific 510(k) clearance for this event. Product: KayserBetten model IDA beds Product Usage: BED, AC-POWERED ADJUSTABLE HOSPITAL. Reason: Some joints on the doors of a limited number of IDA beds may loosen or separate over time which can cause the doors to drop outward and cause injury..

Recalling firm
mobility unlimited inc
Classification
Class II
Status
Terminated
Initiated
2013-04-11
Terminated
2014-10-08
Firm location
Allentown, PA, United States

Product description

KayserBetten model IDA beds Product Usage: BED, AC-POWERED ADJUSTABLE HOSPITAL

Reason for recall

Some joints on the doors of a limited number of IDA beds may loosen or separate over time which can cause the doors to drop outward and cause injury.

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