BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GEMINI PC1CE, 220V AUST

    MDR report key: 328678 · Received April 19, 2001

    Report

    Report Number
    2016493-2001-00064
    Event Type
    Malfunction
    Date Received
    April 19, 2001
    Date of Event
    January 21, 2000
    Report Date
    April 17, 2001
    Manufacturer
    ALARIS MEDICAL SYSTEMS
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE OCCURRENCE OF 161, 162, AND 163 ERROR CODES INDICATING PUMP MOTOR STALLS HAD OCCURRED DURING CLINICAL USE IN 2000. WHILE EXACT USE CONDITIONS ARE NOT AVAILABLE, IT IS BELIEVED THAT THE EVENT WAS NOTED AT FLOW RATES <20ML/HR. THE PT WAS REPORTEDLY NOT INJURED BY THE EVENTS DESPITE THE NOTED USE OF INOTROPIC AGENTS. THE ALARM SYSTEMS REPORTEDLY FUNCTIONED AS INTENDED, NOTIFYING THE CAREGIVERS OF THE EVENTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    17791 GEMINI PC1CE, 220V AUST INFUSION PUMP/CONTROLLER FRN ALARIS MEDICAL SYSTEMS 1311AX01AA *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN