BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CONSULTA CRT-P

    MDR report key: 3863166 · Received June 10, 2014

    Report

    Report Number
    2182208-2014-01668
    Event Type
    Injury
    Date Received
    June 10, 2014
    Date of Event
    March 21, 2014
    Report Date
    March 21, 2014
    Manufacturer
    MEDTRONIC
    Product Code
    NVZ
    PMA / PMN Number
    P010015
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    LG
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS EVENT OCCURRED OUTSIDE THE US. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. PATIENT INFORMATION IS NOT GENERALLY AVAILABLE DUE TO CONFIDENTIALITY CONCERNS. WITHOUT A LOT NUMBER OR DEVICE SERIAL NUMBER, THE MANUFACTURING DATE CANNOT BE DETERMINED. THIS MODEL NUMBER IS NOT APPROVED FOR DISTRIBUTION IN THE UNITED STATES, HOWEVER, IT IS SIMILAR TO A DEVICE MARKETED IN THE U.S. THE EVENT IS BEING REPORTED DUE TO AN ALLEGED MALFUNCTION. (B)(4).

    Description of Event or Problem · 1

    IT WAS REPORTED THAT SIX MONTHS AFTER IMPLANT THERE WAS NO DIAGNOSTIC DATA STORED. THE PATIENT WAS IN PERMANENT ATRIAL FIBRILLATION (AF) AND NO ATRIAL LEAD WAS CONNECTED. THE DEVICE WAS REPROGRAMMED TO IMPLANT DETECT "OFF" AND THE ISSUE WAS SOLVED. THE DEVICE 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
    341107 CONSULTA CRT-P PULSE GENERATOR, PERMANENT, IMPLANTABLE NVZ MEDTRONIC C3TR01

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention