BEUDAMED
    FDA Adverse Event Summary report: N

    MECHANICAL WALKER, ROLLATOR

    MDR report key: 3965099 · Received July 29, 2014

    Report

    Report Number
    1531186-2014-02852
    Date Received
    July 29, 2014
    Date of Event
    June 16, 2014
    Report Date
    June 24, 2014
    Manufacturer
    JUNCHENG
    Product Code
    ITJ
    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

    DEALER ADVISED FRONT RIGHT LEG GAVE IN CAUSING FRAME TO BEND IN WHICH CAUSED IT TO CRACK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    440907 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ JUNCHENG 6240-JR5F

    Patients

    Seq Age Sex Outcome Treatment
    1 Other