BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWERED PATIENT ROTATION BED

    MDR report key: 3212034 · Received July 8, 2013

    Report

    Report Number
    1525712-2013-05462
    Event Type
    Malfunction
    Date Received
    July 8, 2013
    Report Date
    June 14, 2013
    Manufacturer
    UNKNOWN
    Product Code
    IKZ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    THE END USER STATED THE BED WASN'T WORKING CORRECTLY AND WOULD NOT RAISE EVENLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    308974 POWERED PATIENT ROTATION BED 890.5225 IKZ UNKNOWN UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Other