BEUDAMED
    FDA Adverse Event Summary report: N

    PALL

    MDR report key: 273487 · Received April 12, 2000

    Report

    Report Number
    MW1018646
    Date Received
    April 12, 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

    BLOOD LEAKING FROM TUBING BELOW AIR VENT. FILTER DEFECTIVE FROM ONSET OF USE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PALL EZ PRIME FILTER CAK PALL BIOMEDICAL PRODUCTS CO. * 918107

    Patients

    Seq Age Sex Outcome Treatment
    1 *