BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DESARA

    MDR report key: 3260975 · Received July 23, 2013

    Report

    Report Number
    3003990090-2013-00193
    Event Type
    Injury
    Date Received
    July 23, 2013
    Date of Event
    May 27, 2008
    Report Date
    July 19, 2013
    Manufacturer
    CALDERA MEDICAL, INC.
    Product Code
    FTL
    PMA / PMN Number
    K072456
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    EVENT WAS REPORTED TO CALDERA MEDICAL BY AN ATTORNEY. LEGAL COMPLAINT STATES THAT PATIENT SUFFERED PAIN, SUFFERING, DISABILITY, IMPAIRMENT, LOSS OF ENJOYMENT OF LIFE, INABILITY TO ENGAGE IN CHOSEN AND NECESSARY ACTIVITIES, AND/ OR ECONOMIC DAMAGES. AS WELL AS LOSS OF CARE, COMFORT, CONSORTIUM, GUIDANCE, SUPPORT, WRONGFUL DEATH IMAGES, SURVIVORSHIP DAMAGES, AND/ OR OTHER LOSSES AND DAMAGES. NO ADDITIONAL INFORMATION WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    343638 DESARA SURGICAL MESH FTL CALDERA MEDICAL, INC. 18761

    Patients

    Seq Age Sex Outcome Treatment
    1 Other