BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ABBOTT AMBULATORY INFUSION-AIM PLUS PUMP

    MDR report key: 224706 · Received May 14, 1999

    Report

    Report Number
    2024064-1999-00015
    Event Type
    Malfunction
    Date Received
    May 14, 1999
    Date of Event
    April 10, 1999
    Report Date
    April 12, 1999
    Manufacturer
    ABBOTT LABORATORIES, INC.
    Product Code
    FRN
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    NURSE

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT AMBULATORY INFUSION-AIM PLUS PUMP INFUSION PUMP FRN ABBOTT LABORATORIES, INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 71 YR Other