BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ABBOTT INFUSION PUMP

    MDR report key: 306484 · Received November 28, 2000

    Report

    Report Number
    306484
    Event Type
    Injury
    Date Received
    November 28, 2000
    Date of Event
    November 7, 2000
    Report Date
    November 27, 2000
    Manufacturer
    ABBOTT LABORATORIES, INC
    Product Code
    FRN
    Report Source
    User Facility report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    APPROX 700CC IV FLUID INFUSED IN ONE HOUR EVEN THOUGH PUMP WAS SET AT 75 CC/HR AND THE INFUSED VOLUME ON THE PUMP READOUT SHOWED 304CC. IN THE IV, FLUIDS WAS 20MEG POTASSIUM CHLORIDE. CO REP NOTIFIED SHORTLY AFTER INCIDENT BY BIO-MED. A STAT LEVEL OF POTASSIUM WAS DRAWN AT THE TIME OF INCIDENT - WAS NOT REPEATED PRIOR TO DISCHARGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT INFUSION PUMP INFUSION PUMP FRN ABBOTT LABORATORIES, INC PLUM XLD *

    Patients

    Seq Age Sex Outcome Treatment
    1 26 YR Life Threatening| O