BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PLUM A+3 PUMP

    MDR report key: 1951046 · Received December 31, 2010

    Report

    Report Number
    MW5018851
    Event Type
    Injury
    Date Received
    December 31, 2010
    Date of Event
    December 31, 2010
    Report Date
    December 31, 2010
    Manufacturer
    HOSPIRA INC
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OR, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    THE PT'S NURSE WAS ABSOLUTELY SURE THAT SHE HAD PROGRAMMED THE PUMP AT 0.7 MCG/KG/HR, BUT WHEN SHE WENT BACK TO CHECK ON THE PT, THE PUMP SOMEHOW WAS INFUSING ALL THE MEDICATION - PRECEDEX - WITHIN MINUTES. THE NURSE LOOKED AT THE PUMP WHEN IT FINISHED AND IT SHOWED THAT THE PUMP WAS RUNNING 10 MCG/KG/HR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PLUM A+3 PUMP SEDATIVE MED PUMP FRN HOSPIRA INC CUSTOM SWL AG132 18649011

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Life Threatening