BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWERED PATIENT ROTATION BED

    MDR report key: 3200522 · Received July 1, 2013

    Report

    Report Number
    1031452-2013-01245
    Event Type
    Malfunction
    Date Received
    July 1, 2013
    Report Date
    June 7, 2013
    Manufacturer
    INVACARE FLORIDA OPERATIONS
    Product Code
    OSI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    PROVIDER STATES THE CASTERS WOULDN'T NOT LOCK, SO THE BED WOULD MOVE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    298353 POWERED PATIENT ROTATION BED 890.5225 OSI INVACARE FLORIDA OPERATIONS BAR600

    Patients

    Seq Age Sex Outcome Treatment
    1 Other