BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWERED WHEELCHAIR

    MDR report key: 4113054 · Received September 24, 2014

    Report

    Report Number
    1525712-2014-06249
    Event Type
    Malfunction
    Date Received
    September 24, 2014
    Report Date
    September 3, 2014
    Manufacturer
    UNKNOWN
    Product Code
    ITI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    DEALER STATES, BOTH PIVOT SLIDE TUBES ARE BENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    593247 POWERED WHEELCHAIR 890.3860 ITI UNKNOWN 3GTQSP

    Patients

    Seq Age Sex Outcome Treatment
    1 Other