BEUDAMED
    FDA Adverse Event Injury Summary report: N

    IDENTITY ADX SR

    MDR report key: 1073407 · Received July 11, 2008

    Report

    Report Number
    2017865-2008-02196
    Event Type
    Injury
    Date Received
    July 11, 2008
    Date of Event
    April 30, 2008
    Manufacturer
    ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
    Product Code
    DXY
    PMA / PMN Number
    PMA00001
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    FINAL ANALYSIS FOUND A REVERSED MOUNTED CAPACITOR HAD CAUSED HIGH CURRENT DRAIN, RESULTING IN PREMATURE BATTERY DEPLETION.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PULSE GENERATOR EXHIBITED HIGH CURRENT DRAIN AND PREMATURE BATTERY DEPLETION SHORTLY AFTER IMPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IDENTITY ADX SR IMPLANTABLE PACEMAKER PULSE GENERATOR DXY ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION 5180 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention