BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ABBOTT

    MDR report key: 277812 · Received May 11, 2000

    Report

    Report Number
    MW1018891
    Event Type
    Malfunction
    Date Received
    May 11, 2000
    Date of Event
    April 27, 2000
    Report Date
    May 11, 2000
    Manufacturer
    ABBOTT LABORATORIES
    Product Code
    MEA
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NC, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    PT CONTROL CABLE INTERMITTENTLY SHORTED AND ALLOWED UNIT TO CYCLE UNINTENTIONALLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT PCA PUMP MEA ABBOTT LABORATORIES PCA PLUS II LIFECARE 4100 *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other