BEUDAMED
    FDA Adverse Event Other Summary report: N

    HEARTMATE II LVS

    MDR report key: 2495712 · Received March 19, 2012

    Report

    Report Number
    2495712
    Event Type
    Other
    Date Received
    March 19, 2012
    Report Date
    March 19, 2012
    Manufacturer
    THORATEC CORPORATION
    Product Code
    DSQ
    Report Source
    User Facility report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    MAJOR PUMP UNIT(S) INVOLVED: BLOOD PUMP. SPECIFIC COMPONENT(S)INVOLVED: PUMP DRIVER UNIT MALFUNCTION.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1