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.