BEUDAMED
    FDA Adverse Event Summary report: N

    MECHANICAL (MANUAL) WHEELCHAIR

    MDR report key: 3840991 · Received May 30, 2014

    Report

    Report Number
    1531186-2014-02028
    Date Received
    May 30, 2014
    Date of Event
    April 13, 2014
    Report Date
    April 15, 2014
    Manufacturer
    JUMAO MEDICAL EQUIPMENT
    Product Code
    IOR
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    DEALER REPORTED THAT END USER STATED THAT THE LEFT REAR WHEEL ON HIS (B)(4) WHEELCHAIR BINDS, AT TIMES, MAKING IT HARD FOR A HANDLER TO MANEUVER THE CHAIR AND ALMOST IMPOSSIBLE FOR THE USER TO MANEUVER THE CHAIR HIMSELF.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    317859 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO MEDICAL EQUIPMENT V18RLR

    Patients

    Seq Age Sex Outcome Treatment
    1 Other