BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HEARTMATE II LVAS

    MDR report key: 3013256 · Received March 20, 2013

    Report

    Report Number
    3013256
    Event Type
    Injury
    Date Received
    March 20, 2013
    Date of Event
    March 11, 2013
    Report Date
    March 20, 2013
    Manufacturer
    THORATEC CORPORATION
    Product Code
    DSQ
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PATIENT HAD ELEVATED LDH LAB VALUES ALONG WITH PUMP POWER SPIKES. IT WAS DETERMINED TO HAVE THE DEVICE EXCHANGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    115865 HEARTMATE II LVAS LVAD DSQ THORATEC CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1