BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NA

    MDR report key: 2181287 · Received July 21, 2011

    Report

    Report Number
    MW5021489
    Event Type
    Injury
    Date Received
    July 21, 2011
    Date of Event
    July 21, 2011
    Report Date
    July 21, 2011
    Manufacturer
    NA
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    SURGICAL INTERVENTION FOR VAGINAL EROSION FROM IMPLANTED MESH. TRANSOBTURATOR SLING PERFORMED ORIGINAL SURGERY IN 2007. DATES OF USE: (B)(6) 2007 - (B)(6) 2011. REASON FOR USE: STRESS URINARY INCONTINENCE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NA MESH FTL NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 47 YR Hospitalization