BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DESARA

    MDR report key: 2980662 · Received February 20, 2013

    Report

    Report Number
    3003990090-2012-00109
    Event Type
    Injury
    Date Received
    February 20, 2013
    Date of Event
    June 16, 2011
    Report Date
    January 7, 2013
    Manufacturer
    CALDERA MEDICAL, INC.
    Product Code
    FTL
    PMA / PMN Number
    K101169
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, 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, EROSION, URINARY PROBLEMS, RECURRENCE, AND DYSPAREUNIA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    74052 DESARA SURGICAL MESH FTL CALDERA MEDICAL, INC. DESARA 012003

    Patients

    Seq Age Sex Outcome Treatment
    1 Other