BEUDAMED
    FDA Adverse Event Other Summary report: N

    ALARIS 8100

    MDR report key: 17720029 · Received September 8, 2023

    Report

    Report Number
    MW5145455
    Event Type
    Other
    Date Received
    September 8, 2023
    Date of Event
    September 5, 2023
    Report Date
    September 5, 2023
    Manufacturer
    CAREFUSION 303, INC.
    Product Code
    FRN
    Report Source
    Voluntary report
    Reporter Location
    VA, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    RATE OF DIPRIVAN INFUSING AT 0632 ON (B)(6) 2023 WAS 35 MCG/KG/MIN. AROUND 0710, BSSR COMPLETED AND DIPRIVAN BOTTLE NOTICED TO HAVE INFUSED ALMOST ALL OF THE BOTTLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2061940 ALARIS 8100 PUMP, INFUSION FRN CAREFUSION 303, INC. 8100

    Patients

    Seq Age Sex Outcome Treatment
    1 75 YR Female