BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BED, MANUAL

    MDR report key: 3143720 · Received June 3, 2013

    Report

    Report Number
    1031452-2013-01036
    Event Type
    Malfunction
    Date Received
    June 3, 2013
    Report Date
    May 7, 2013
    Manufacturer
    INVACARE FLORIDA OPERATIONS
    Product Code
    OSI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    CONSUMER ALLEGES THAT HE HAD TO PLAY WITH THE CORD FOR THE BED TO WORK. IT HAS BEEN SWITCHED 2 TIMES AND NOW IT DOES NOT WORK AT ALL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    243648 BED, MANUAL 880.5120 OSI INVACARE FLORIDA OPERATIONS BAR600

    Patients

    Seq Age Sex Outcome Treatment
    1 Other