BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ABBOTT

    MDR report key: 297230 · Received September 20, 2000

    Report

    Report Number
    MW1019964
    Event Type
    Malfunction
    Date Received
    September 20, 2000
    Date of Event
    September 4, 2000
    Report Date
    September 8, 2000
    Manufacturer
    ABBOTT
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IV PUMP CONTINUED TO DISPLAY MALFUNCTION CODE, EVEN AFTER THE CASSETTE HOLDER, ESPECIALLY THE PRONGS, WAS CLEANED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT IV PUMP FRN ABBOTT * *

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Other