BEUDAMED
    FDA Adverse Event Other Summary report: N

    ALARIS

    MDR report key: 17660674 · Received August 31, 2023

    Report

    Report Number
    17660674
    Event Type
    Other
    Date Received
    August 31, 2023
    Date of Event
    August 18, 2023
    Report Date
    August 22, 2023
    Manufacturer
    CAREFUSION 303, INC.
    Product Code
    FRN
    Report Source
    User Facility report
    Reporter Location
    CA
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PUMP/BRAIN BUTTONS NOT WORKING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1390052 ALARIS PUMP, INFUSION FRN CAREFUSION 303, INC. 8015

    Patients

    Seq Age Sex Outcome Treatment
    1 44530 DA Unknown