BEUDAMED
    FDA Adverse Event Other Summary report: N

    HEARTMATE II LVAS

    MDR report key: 3088434 · Received May 1, 2013

    Report

    Report Number
    3088434
    Event Type
    Other
    Date Received
    May 1, 2013
    Date of Event
    April 22, 2013
    Report Date
    April 27, 2013
    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

    LOW FLOW ALARMS SUDDENLY RESOLVING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    189741 HEARTMATE II LVAS LVAD DSQ THORATEC CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1