BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MECHANICAL WALKER, ROLLATOR

    MDR report key: 3935138 · Received July 15, 2014

    Report

    Report Number
    1525712-2014-03687
    Event Type
    Malfunction
    Date Received
    July 15, 2014
    Report Date
    June 9, 2014
    Manufacturer
    UNKNOWN
    Product Code
    ITJ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    PER PROVIDER ORIGINAL 861497294, CUSTOMER STATES THESE KNOBS FOR THE ARM HEIGHT ADJUSTMENT WERE NOT IN THE BOX WITH THE PRODUCT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    411992 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN SELFCARE

    Patients

    Seq Age Sex Outcome Treatment
    1 Other