BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE

    MDR report key: 3042216 · Received April 4, 2013

    Report

    Report Number
    2916596-2013-00339
    Event Type
    Injury
    Date Received
    April 4, 2013
    Date of Event
    March 6, 2013
    Report Date
    March 6, 2013
    Manufacturer
    THORATEC CORP.
    Product Code
    DSQ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE PATIENT REMAINS ON GOING WITH THE IMPLANTED DEVICE. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME. A SUPPLEMENTAL REPORT WILL BE SUBMITTED WHEN THE MFR'S INVESTIGATION IS COMPLETED.

    Description of Event or Problem · 1

    THE PATIENT WAS IMPLANTED WITH A LEFT VENTRICULAR ASSIST DEVICE. THE VAD COORDINATOR REPORTED THAT PATIENT WAS IN THE EMERGENCY DEPARTMENT "CODING". HE WAS RESUSCITATED WITH FRESH FROZEN PLASMA AND PERMEABLE REACTIVE BARRIERS EMERGENTLY. REPORTED TO HAVE DARK BLACK EMESIS, BUT NO OTHER SOURCES OF BLEEDING WERE FOUND. THE PATIENT WAS ALSO SUSPECTED TO BE ASPIRATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    139209 HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE DSQ: LEFT VENTRICULAR ASSIST DEVICE DSQ THORATEC CORP. 104911 123083

    Patients

    Seq Age Sex Outcome Treatment
    1 79 YR Required Intervention