BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SILICONE INJECTIONS

    MDR report key: 1032534 · Received April 9, 2008

    Report

    Report Number
    MW5006333
    Event Type
    Injury
    Date Received
    April 9, 2008
    Date of Event
    June 15, 2002
    Report Date
    April 8, 2008
    Product Code
    KGM
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    "HI, I WAS INJECTED WITH SILICONE INJECTIONS IN 2002 WHEN A FRIEND TOOK ME TO A PLACE WHERE SHE WAS GETTING SOME INJECTIONS, THIS STUPID LADY TELL ME THAT YOU DON'T DO THE INJECTIONS TO AND I SAY I SCARE, AND SHE SAY IS NOTHING TO SCARE EVERYTHING BE FINE AND NOW I FELL SOME PAIN AND MY HIPS CLOSE TO THE BUTTOCK AREA WHERE THIS WOMAN INJECTED ME. I DON'T KNOW WHY, BUT AND AFTER I WAS READING FOR INFORMATION IN THE COMPUTER, I CAN'T BELIEVE THAT WOMAN LIE TO ME, AND I'M SO SAD HOW CAN DOCTORS REMOVE THAT PLEASE HELP IM ON PAIN NOW RECOMMEND SOME DOCTORS I CAN BELIEVE I PASSING FOR THIS".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SILICONE INJECTIONS NONE KGM

    Patients

    Seq Age Sex Outcome Treatment
    1 20 YR Life Threatening