BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ESSURE

    MDR report key: 3781417 · Received April 30, 2014

    Report

    Report Number
    MW5035823
    Event Type
    Injury
    Date Received
    April 30, 2014
    Date of Event
    July 10, 2013
    Report Date
    April 16, 2014
    Manufacturer
    BAYER
    Product Code
    HHS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    ONE OF THE DEVICE MIGRATED OUT OF MY BODY AND THE FOLLOWING WEEK FOUND OUT I WAS EXPECTING 5 WEEKS ALREADY. (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    260152 ESSURE HHS BAYER

    Patients

    Seq Age Sex Outcome Treatment
    1 39.000 YR Other PREGNANCY