BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRILOGY SR

    MDR report key: 4142986 · Received January 13, 2014

    Report

    Report Number
    2017865-2014-05599
    Event Type
    Malfunction
    Date Received
    January 13, 2014
    Date of Event
    December 13, 2011
    Manufacturer
    ST. JUDE MEDICAL, CRMD
    Product Code
    DXY
    PMA / PMN Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS HISTORICAL COMPLAINT IS BEING FILED AS PART OF A RETROSPECTIVE REVIEW OF COMPLAINT FILES IN RESPONSE TO A RECENT FDA INSPECTION. THERE IS NO CHANGE TO THE ACTUAL PERFORMANCE OF THE PRODUCT AND THIS REPORT ONLY REPRESENTS AN ENHANCEMENT TO THE REPORTING CRITERIA GOING FORWARD.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PT PRESENTED TO THE HOSP. THE PULSE GENERATOR EXHIBITED LOSS OF CAPTURE. THE DEVICE WAS CLINICALLY RESOLVED BY REPROGRAMMING. THE DEVICE REMAINED IMPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    31661 TRILOGY SR IMPLANTABLE PACEMAKER PULSE GENERATOR DXY ST. JUDE MEDICAL, CRMD 2260L

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR