BEUDAMED
    FDA Adverse Event Death Summary report: N

    CADENCE V-110 SERIES TIERED THERAPY DEFIBRILLATOR

    MDR report key: 206599 · Received January 20, 1999

    Report

    Report Number
    2938836-1999-00027
    Event Type
    Death
    Date Received
    January 20, 1999
    Date of Event
    November 21, 1995
    Report Date
    November 21, 1995
    Manufacturer
    *
    Product Code
    LWS
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    AS A RESULT OF THE PRODUCT NOTIFICATION EFFORT UNDER RECALL Z-232-7, ST JUDE MEDICAL LEARNED THAT THIS PERSON HAD DIED. NO DETAILS REGARDING CAUSE OF DEATH WERE ATTAINABLE FROM THE PHYSICIANS. ST. JUDE SUBSEQUENTLY REQUESTED AND REC'D A DEATH CERTIFICATE. THE CERTIFICATE LISTS VENTRICULAR TACHYCARDIA/FIBRILLATION AS THE IMMEDIATE CAUSE OF DEATH WITH DILATED CARDIOMYOPATHY AND MITRAL VALVE AS CONIDITIONS LEADING TO THE VENTRICULAR TACHYCARDIA. THIS PERSON DIED AS AN INPATIENT, AND THERE HAS BEEN NO REPORT FROM THE USER FACILITY THAT THE DEVICE HAD FAILED TO CONVERT AN ARRHYTHMIA. CO IS, HOWEVER, REPORTING THE DEATH BECAUSE CO HAS NEITHER THE DEVICE NOR ANY ASSOCIATED DATA OR ELECTROGRAMS WHICH WOULD ENABLE CO TO CONCLUDE THAT THE DEVICE DID NOT CONTRIBUTE TO THE DEATH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CADENCE V-110 SERIES TIERED THERAPY DEFIBRILLATOR Implant IMPLANTABLE CARDIAC DEFIBRILLATOR LWS * V-110C NA

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Death CPI 0072, THERAPY DATES: NA.