BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWERED PATIENT ROTATION BED

    MDR report key: 3013789 · Received March 20, 2013

    Report

    Report Number
    1031452-2013-00584
    Event Type
    Malfunction
    Date Received
    March 20, 2013
    Report Date
    February 21, 2013
    Manufacturer
    INVACARE FLORIDA OPERATIONS
    Product Code
    IKZ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    PROVIDER ALLEGES THE BED WOULD MOVE ON ITS OWN WHEN PLUGGED IN. PROVIDER ALLEGES WHEN HE WENT OUT TO LOOK AT THE BED AND THEY PLUGGED IT BACK IN IT NOW WILL NOT MOVE AT ALL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    115431 POWERED PATIENT ROTATION BED 890.5225 IKZ INVACARE FLORIDA OPERATIONS BED10-1633

    Patients

    Seq Age Sex Outcome Treatment
    1 Other