BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TERUMO PERFUSION SYSTEM 8000

    MDR report key: 1002082 · Received February 20, 2008

    Report

    Report Number
    1828100-2008-00098
    Event Type
    Malfunction
    Date Received
    February 20, 2008
    Date of Event
    January 21, 2008
    Report Date
    February 20, 2008
    Manufacturer
    TERUMO CARDIOVASCULAR SYSTEMS CORP.
    Product Code
    DTQ
    PMA / PMN Number
    K915183
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BE
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    EVALUATION IN PROGRESS, BUT NOT CONCLUDED.

    Description of Event or Problem · 1

    DURING USE OF THE DEVICE IN A CARDIOPULMONARY BYPASS PROCEDURE, THE USER REPORTED THAT ROLLER PUMP STOPPED, DISPLAYING AN "OVERSPEED" ERROR MESSAGE. NO PT INJURY WAS REPORTED AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TERUMO PERFUSION SYSTEM 8000 ROLLER PUMP DTQ TERUMO CARDIOVASCULAR SYSTEMS CORP. 16395

    Patients

    Seq Age Sex Outcome Treatment
    1