BEUDAMED
    FDA Adverse Event Summary report: N

    MAGIC MOBILITY

    MDR report key: 7040932 · Received November 16, 2017

    Report

    Report Number
    MW5073396
    Date Received
    November 16, 2017
    Date of Event
    September 12, 2017
    Report Date
    November 15, 2017
    Manufacturer
    MAGIC MOBILITY
    Product Code
    ITI
    Report Source
    Voluntary report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PATIENT USED HIS POWER WHEELCHAIR AS A GROUND FOR HIS WELDER. THIS CREATED A MAJOR OVERCURRENT CAUSING THE CHAIR TO SHORT AND THE WIRING TO MELT. THE WHEELCHAIR CANNOT BE TESTED DUE TO THE EXTENSIVE DAMAGE TO THE CHAIR. THE POWER WHEELCHAIR IS UNFIT FOR USE AND HAS BEEN CONDEMNED. NO OTHER ISSUES HAVE BEEN REPORTED FOR THIS POWER WHEELCHAIR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    815552 MAGIC MOBILITY EXTREME X8 ITI MAGIC MOBILITY

    Patients

    Seq Age Sex Outcome Treatment
    1