BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SILICONE BREAST IMPLANTS LEFT - NATRELLE INSPIRA

    MDR report key: 19172044 · Received April 23, 2024

    Report

    Report Number
    MW5154135
    Event Type
    Injury
    Date Received
    April 23, 2024
    Date of Event
    September 1, 2023
    Report Date
    April 20, 2024
    Manufacturer
    ALLERGAN SALES, LLC.
    Product Code
    FTR
    UDI-DI
    10888628007369
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I GOT SILICONE BREAST IMPLANTS AND MY DOCTOR THOUGHT I HAD CANCER (LYMPHOMA) AND I HAD TO GET UNNECESSARY SURGERY FOR TESTING. THESE ARE POISON PLEASE MAKE THIS AN OFFICIAL MEDICAL DIAGNOSIS OR TAKE THESE POISONOUS PRODUCTS OFF THE MARKET. THEY RUINED MY LIFE WITH PERMANENT AUTOIMMUNE DISEASE. REFERENCE REPORT: MW5154136.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    982823 SILICONE BREAST IMPLANTS LEFT - NATRELLE INSPIRA PROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED FTR ALLERGAN SALES, LLC. 10888628007369

    Patients

    Seq Age Sex Outcome Treatment
    1 20 YR Female Other| S| H