BEUDAMED
    FDA Adverse Event Summary report: N

    MECHANICAL WALKER, ROLLATOR

    MDR report key: 2921374 · Received January 17, 2013

    Report

    Report Number
    1531186-2013-00234
    Date Received
    January 17, 2013
    Report Date
    January 17, 2013
    Manufacturer
    JUNCHENG
    Product Code
    ITJ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    DEALER STATED THAT THE FRAME ON A 6240-5F WALKER IS BENT AT THE RELEASE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    26593 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ JUNCHENG 6240-5F

    Patients

    Seq Age Sex Outcome Treatment
    1 Other