BEUDAMED
    FDA Adverse Event Summary report: N

    UNKNOWN - BLANK

    MDR report key: 395784 · Received May 21, 2002

    Report

    Report Number
    1314412-2002-00006
    Date Received
    May 21, 2002
    Report Date
    May 21, 2002
    Manufacturer
    THE KENDAL CO.
    Product Code
    FPD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    KENDALL RECEIVED A COMPLAINT ALLEGING THAT WHEN PASSING A FEEDING TUBE, PERFORATION OF THE PLEURAL TISSUE OCCURRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNKNOWN - BLANK * FPD THE KENDAL CO. * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention