MalfunctionFMW
XPRT SLEEP SURFACE
Received Mar 5, 2013 · Event occurred Feb 7, 2013
Report 0001831750-2013-01715 · MDR key 2988742
Device
Generic name
Bed, Patient Rotation, Powered
Manufacturer
Stryker Medical-kalamazooCatalog number
2950000000
Product problems
- Device Operates Differently Than Expected
Patient
Not reported
- No Consequences Or Impact To Patient
Narrative
Description of Event or Problem
IT WAS REPORTED BY REPAIR WORK ORDER THAT THE MATTRESS HAD FLUID INGRESS. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.