BEUDAMED
    FDA Adverse Event Summary report: N

    ALARIS

    MDR report key: 1900982 · Received October 15, 2010

    Report

    Report Number
    1900982
    Date Received
    October 15, 2010
    Date of Event
    October 15, 2010
    Report Date
    October 15, 2010
    Manufacturer
    CAREFUSION
    Product Code
    FRN
    Report Source
    User Facility report
    Reporter Location
    AZ, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    INFUSION PUMP ALARMED AND RED LIGHT NOTED. INFUSION HAD STOPPED, UNABLE TO RESTART; THE PUMP HAD TO BE REPLACED WITH ANOTHER PUMP.====================== HEALTH PROFESSIONAL'S IMPRESSION======================DID NOT KNOW THE CAUSE - NO ADVERSE EVENT TO PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ALARIS INFUSION PUMP FRN CAREFUSION * *

    Patients

    Seq Age Sex Outcome Treatment
    1 48 YR