BEUDAMED
    FDA Adverse Event Summary report: N

    *

    MDR report key: 276150 · Received May 2, 2000

    Report

    Report Number
    MW1018791
    Date Received
    May 2, 2000
    Report Date
    May 2, 2000
    Manufacturer
    PALL BIOMEDICAL PRODUCTS CO.
    Product Code
    CAK
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    COULD NOT PRIME BOTH SIDES OF FILTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * EZ PRIME LEUKOCYTE FILTER CAK PALL BIOMEDICAL PRODUCTS CO. * 907606

    Patients

    Seq Age Sex Outcome Treatment
    1 *