BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CAREFUSION

    MDR report key: 2442446 · Received February 2, 2012

    Report

    Report Number
    MW5024155
    Event Type
    Injury
    Date Received
    February 2, 2012
    Date of Event
    January 27, 2012
    Report Date
    February 2, 2012
    Product Code
    FRN
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT ON EPINEPHRINE AND PROPOFOL INFUSIONS WHEN ALARIS PUMP ALARMED AND PROVIDED A SYS OUTAGE MESSAGE. NO SIGNIFICANT CHANGE IN MAP.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 78 YR Disability