BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AIM PLUS

    MDR report key: 232038 · Received July 13, 1999

    Report

    Report Number
    MW1016737
    Event Type
    Injury
    Date Received
    July 13, 1999
    Date of Event
    July 13, 1999
    Report Date
    July 13, 1999
    Manufacturer
    ABBOTT LABORATORIES, INC.
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT ON CONTINUOUS MILRINONE THERAPY. PUMP ALARMED "ERROR 9". (PUMP NOT PUMPING) REPEATEDLY. PT WAS DISCONNECTED FROM PUMP AND A NEW PUMP WAS DELIVERED TO PT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Required Intervention