BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ABBOTT

    MDR report key: 276856 · Received May 3, 2000

    Report

    Report Number
    276856
    Event Type
    Malfunction
    Date Received
    May 3, 2000
    Date of Event
    April 12, 2000
    Report Date
    May 1, 2000
    Manufacturer
    ABBOTT HOSPITAL PRODUCTS DIVISION
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    INFUSION PUMP, REPORTED BY NURSING UNIT, DELIVERED EXCESSIVE AMOUNT OF MORPHINE TO PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT INFUSION PUMP FRN ABBOTT HOSPITAL PRODUCTS DIVISION 5000 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *