BEUDAMED
    FDA Adverse Event Injury Summary report: N

    THORATEC PVAD

    MDR report key: 2923386 · Received January 22, 2013

    Report

    Report Number
    2923386
    Event Type
    Injury
    Date Received
    January 22, 2013
    Date of Event
    January 13, 2013
    Report Date
    January 18, 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 AN ALARM "RVAD OCCLUSION" AT HOME WITH LOSS OF FLASH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    30724 THORATEC PVAD BIVAD DSQ THORATEC CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1