BEUDAMED
    FDA Adverse Event Death Summary report: N

    SECURA DR

    MDR report key: 2071189 · Received April 27, 2011

    Report

    Report Number
    2647346-2011-00610
    Event Type
    Death
    Date Received
    April 27, 2011
    Date of Event
    February 18, 2011
    Manufacturer
    MEDTRONIC MED REL, INC.
    Product Code
    LWS
    PMA / PMN Number
    P980016/S114
    Removal / Correction Number
    ASKU
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT DIED ON THE DAY OF IMPLANT OF AN IMPLANTABLE CARDIAC DEFIBRILLATOR AND RIGHT VENTRICULAR LEAD. FOLLOW UP REVEALED THAT THE SURGERY WAS ROUTINE, THE PATIENT WAS TRANSPORTED TO THE POST OPERATION ROOM, AND THEN DIED OF RESPIRATORY FAILURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURA DR IMPLANTABLE PACEMAKER/CARDIO/DEFIB LWS MEDTRONIC MED REL, INC. D224DRG ASKU

    Patients

    Seq Age Sex Outcome Treatment
    1 63 YR Death| H| L| R