BEUDAMED
    FDA Adverse Event Other Summary report: N

    CORFLO

    MDR report key: 469616 · Received July 3, 2003

    Report

    Report Number
    1419949-2003-00014
    Event Type
    Other
    Date Received
    July 3, 2003
    Date of Event
    June 25, 2003
    Report Date
    July 1, 2003
    Manufacturer
    VIASYS MEDSYSTEMS
    Product Code
    FPD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    FEEDING TUBE WAS FOUND TO HAVE BEEN PASSED INTO LUNGS. TUBE REMOVED AND DISCARDED. PATIENT HAD NOT BEEN FED. NO RESPIRATORY DISTRESS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CORFLO ENTERAL FEEDING TUBE FPD VIASYS MEDSYSTEMS NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention