BEUDAMED
    FDA Adverse Event Death Summary report: N

    ESSURE

    MDR report key: 21491863 · Received February 28, 2025

    Report

    Report Number
    MW5167052
    Event Type
    Death
    Date Received
    February 28, 2025
    Date of Event
    June 1, 2011
    Report Date
    February 26, 2025
    Manufacturer
    BAYER HEALTHCARE, LLC.
    Product Code
    HHS
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    ON (B)(6) 2011 DR. (B)(6) IN (B)(6) AND SHE WORKED FOR (B)(6) HOSPITAL IN (B)(6). SHE AIN'T PLAYING ME WITH THE BIRTH CONTROL DEVICE CALLED ESSURE BIRTH CONTROL THEIR TWO RODS THEY'RE STUCK IN MY FALLOPIAN TUBES ON (B)(6) AT 2011 SHE KNEW THEY WOULD BE RECALLED IN 2008, BUT SHE STILL PUT THEM INSIDE ME IN 2017 I HAD A YOUNG DAUGHTER ON (B)(6) 2017 I HAD A DAUGHTER BORN WITHOUT REPRODUCTIVE PARTS. I WAS NOT SUPPOSED TO HAVE A BABY (B)(6) OF 2018 I GAVE BIRTH TO A STILLBORN BABY WHO WAS BORN WITHOUT REPRODUCTIVE ORGANS, AND SHE DIED 6 HOURS LATER AFTER GIVING ME HER LAST BREATH I AM CURRENTLY LIVING IN (B)(6) WITHOUT MY FALLOPIAN TUBES AND MY OVARIES. DR (B)(6) OF (B)(6) HOSPITAL IN (B)(6) REMOVED THE DETECTED AND CORRODED OVARIES AND MY FALLOPIAN TUBES (B)(6) OF 2019 AND EVER SINCE THEN I'VE BEEN HAVING PROBLEMS IN MY LOWER REGION OF MY PUBLIC AREA AND MY UTERUS AREA. I NEED HELP AND I NEED A LAWYER TO GO AFTER DR (B)(6). REF REPORT: MW5167053.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    690859 ESSURE TRANSCERVICAL CONTRACEPTIVE TUBAL OCCLUSION DEVICE HHS BAYER HEALTHCARE, LLC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Death