BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FIXODENT

    MDR report key: 1407236 · Received June 23, 2009

    Report

    Report Number
    MW5011657
    Event Type
    Injury
    Date Received
    June 23, 2009
    Product Code
    KOL
    Report Source
    Voluntary report
    Reporter Location
    AL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    NO DR SAID IT WAS FROM FIXODENT, BUT I DO HAVE A PROBLEM AND I DO USE IT. BUT I DO HAVE ALL THE PROBLEMS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FIXODENT NONE KOL

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Disability