BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TENDRIL SDX

    MDR report key: 3925829 · Received July 10, 2014

    Report

    Report Number
    2017865-2014-15662
    Event Type
    Injury
    Date Received
    July 10, 2014
    Date of Event
    August 11, 2011
    Manufacturer
    ST. JUDE MEDICAL, INC., CRMD
    Product Code
    NVN
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE RIGHT VENTRICULAR LEAD EXHIBITED INCREASED THRESHOLDS AND IMPEDANCE. AN ECHOCARDIOGRAM REVEALED THAT PERICARDIAL EFFUSION HAD OCCURRED. A LEAD PERFORATION WAS ALSO NOTED. THE LEAD WAS EXPLANTED AND REPLACED ON (B)(6) 2011.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    404557 TENDRIL SDX PERMANENT PACEMAKER ELECTRODE NVN ST. JUDE MEDICAL, INC., CRMD 1688TC/58 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 90 YR Required Intervention