BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MESH SLING

    MDR report key: 2932563 · Received January 25, 2013

    Report

    Report Number
    MW5028742
    Event Type
    Injury
    Date Received
    January 25, 2013
    Date of Event
    October 11, 2010
    Report Date
    January 14, 2013
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    PHYSICIAN ASSISTANT

    Narratives

    Description of Event or Problem · 1

    PT HAD CHRONIC PELVIC PAIN, VAGINAL DISCHARGE AND BLEEDING, DUE TO MESH SLING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    36199 MESH SLING NONE FTL

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Hospitalization