BEUDAMED
    FDA Adverse Event Injury Summary report: N

    URETHRAL SLING

    MDR report key: 1950866 · Received January 3, 2011

    Report

    Report Number
    MW5018831
    Event Type
    Injury
    Date Received
    January 3, 2011
    Date of Event
    October 31, 2010
    Report Date
    January 3, 2011
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NV, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    BLEEDING, PAIN AND EROSION EXPERIENCED AFTER PLACEMENT OF MESH. PT ALSO HAS FREQUENT UTIS. MESH TO BE REMOVED ON (B)(6) 2011.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 URETHRAL SLING FTL

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR Other| R