BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TERUMO CENTRIFUGAL SYSTEM

    MDR report key: 1140845 · Received May 5, 2008

    Report

    Report Number
    1828100-2008-00246
    Event Type
    Malfunction
    Date Received
    May 5, 2008
    Date of Event
    April 10, 2008
    Report Date
    May 5, 2008
    Manufacturer
    TERUMO CARDIOVASCULAR SYSTEMS CORP.
    Product Code
    KFM
    PMA / PMN Number
    K882758
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    DURING CARDIOPULMONARY BYPASS, THE CENTRIFUGAL PUMP STOPPED MOMENTARILY. THE PUMP WAS HAND-CRANKED UNTIL AN ALTERNATE DEVICE WAS EMPLOYED. THE PROCEDURE WAS CONCLUDED WITHOUT INCIDENT. THERE WAS NO ADVERSE CONSEQUENCE TO THE PT AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TERUMO CENTRIFUGAL SYSTEM CENTRIFUGAL PUMP MOTOR KFM TERUMO CARDIOVASCULAR SYSTEMS CORP. 164267 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *