BEUDAMED
    FDA Adverse Event Other Summary report: N

    ABBOTT

    MDR report key: 280901 · Received June 7, 2000

    Report

    Report Number
    280901
    Event Type
    Other
    Date Received
    June 7, 2000
    Date of Event
    April 26, 2000
    Report Date
    May 22, 2000
    Manufacturer
    ABBOTT LABORATORIES
    Product Code
    MEA
    Report Source
    User Facility report
    Reporter Location
    MI, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    PUMP READ MALFUNCTION CODE B, NO INJURY TO PT. PUMP SENT BACK TO ABBOTT FOR ANALYSIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT PCA EPIDURAL PUMP MEA ABBOTT LABORATORIES * *

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR Other