BEUDAMED
    FDA Adverse Event Summary report: N

    MECHANICAL WALKER, ROLLATOR

    MDR report key: 2891990 · Received January 1, 2013

    Report

    Report Number
    1531186-2012-01924
    Date Received
    January 1, 2013
    Report Date
    December 31, 2012
    Manufacturer
    UNKNOWN
    Product Code
    ITJ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    (B)(4) - THE DEALER REPORTED THAT THE 6240-A WALKER WAS BENT IN THE MIDDLE. THERE WAS NO PATIENT INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    84 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 6240-A

    Patients

    Seq Age Sex Outcome Treatment
    1 Other