BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TENDRIL DX

    MDR report key: 1896361 · Received November 10, 2010

    Report

    Report Number
    2017865-2010-04901
    Event Type
    Injury
    Date Received
    November 10, 2010
    Date of Event
    August 20, 2010
    Manufacturer
    ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
    Product Code
    DTB
    PMA / PMN Number
    P960013
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    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 PACEMAKER DEPENDENT PATIENT PRESENTED IN CLINIC, FEELING SYMPTOMATIC. THE VENTRICULAR LEAD APPEARED TO BE OVERSENSING, CAUSING PACING INHIBITION FOR UP TO 1500 MS. THE PHYSICIAN ELECTED TO CAP AND REPLACE THE LEAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TENDRIL DX PERMANENT PACEMAKER ELECTRODE DTB ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION 1388T/58 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 80 YR Required Intervention