BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    AIGIS LARGE

    MDR report key: 3994636 · Received August 8, 2014

    Report

    Report Number
    3005619263-2014-00006
    Event Type
    Malfunction
    Date Received
    August 8, 2014
    Date of Event
    April 2, 2014
    Report Date
    June 3, 2014
    Manufacturer
    TYRX, INC.
    Product Code
    FTL
    PMA / PMN Number
    K063091
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. (B)(4).

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PRODUCT WAS IMPLANTED AFTER ITS "USE-BEFORE-DATE." THE PRODUCT REMAINS IN USE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    471279 AIGIS LARGE MESH, SURGICAL, POLYMERIC FTL TYRX, INC. CMRM3133 12MO4315

    Patients

    Seq Age Sex Outcome Treatment
    1