BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CAREFUSION

    MDR report key: 2497892 · Received February 17, 2012

    Report

    Report Number
    2497892
    Event Type
    Injury
    Date Received
    February 17, 2012
    Date of Event
    December 22, 2012
    Report Date
    February 6, 2012
    Manufacturer
    CAREFUSION
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CALLED BY RECOVERY ROOM DUE TO A PUMP QUESTION. PATIENT WAS SET UP ON AN INSULIN INFUSION IN PRESURG AT 1UNIT/HR. CONFIRMED BY 2 NURSES. ANESTHESIA CAME OUT TO REPORT INFUSION WAS AT 40U/HR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CAREFUSION ALARIS PUMP FRN CAREFUSION 13541126 13523274

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR Required Intervention