BEUDAMED
    FDA Adverse Event Summary report: N

    DOBBHOFF FEEDING TUBE

    MDR report key: 384895 · Received March 21, 2002

    Report

    Report Number
    1314412-2002-00003
    Date Received
    March 21, 2002
    Date of Event
    March 14, 2002
    Report Date
    March 21, 2002
    Manufacturer
    THE KENDAL CO.
    Product Code
    FPD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    WHEN THE FEEDING TUBE WAS REMOVED FROM THE PATIENT THE WEIGHTED END WAS NOT THERE. THE PATIENT'S X-RAY SHOWED THE WEIGHT IN PATIENT'S STOMACH. PATIENT WILL BE CHECKED BY X-RAY TO DETERMINE WHETHER THE WEIGHT HAS BEEN PASSED. NO PATIENT INJURY. KENDALL QA WAS NOTIFIED OF THE INCIDENT ON 03/19/02.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DOBBHOFF FEEDING TUBE * FPD THE KENDAL CO. * U105152

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other