BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ABBOTT

    MDR report key: 217139 · Received April 1, 1999

    Report

    Report Number
    MW1016041
    Event Type
    Malfunction
    Date Received
    April 1, 1999
    Date of Event
    February 11, 1999
    Report Date
    April 1, 1999
    Manufacturer
    ABBOTT LABORATORIES, INC.
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PUMP TUBING CONNECTING CAP DIDN'T FIT ON THE EXTENSION TUBING. IT IS SHAPED WRONG.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT PRIMARY PUMP FRN ABBOTT LABORATORIES, INC. * 44-093NS

    Patients

    Seq Age Sex Outcome Treatment
    1 NA