BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ALARIS

    MDR report key: 4250934 · Received November 7, 2014

    Report

    Report Number
    4250934
    Event Type
    Malfunction
    Date Received
    November 7, 2014
    Date of Event
    June 18, 2014
    Report Date
    November 7, 2014
    Manufacturer
    CAREFUSION CORPORATION
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH, US

    Narratives

    Description of Event or Problem · 1

    HAD HUNG LEVOFLOXACIN USING THE PUMP; HAD TO COMPLETELY TURN PUMP ON AND PROGRAM USING DRUG LIBRARY, SHOULD HAVE DELIVERED OVER 90 MINUTES BUT DELIVERED IN 37 MINUTES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    719651 ALARIS PUMP, INFUSION FRN CAREFUSION CORPORATION * *

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR