BEUDAMED
    FDA Adverse Event Other Summary report: N

    BARD NG TUBE

    MDR report key: 633490 · Received August 22, 2005

    Report

    Report Number
    633490
    Event Type
    Other
    Date Received
    August 22, 2005
    Date of Event
    May 31, 2005
    Report Date
    August 22, 2005
    Manufacturer
    C. R. BARD INC
    Product Code
    FEG
    Report Source
    User Facility report
    Reporter Location
    ME, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    NG, NASOGASTRIC, TUBE PLACEMENT CHECKED BY PHYSICIAN BY AUSCULTATION. ORDER GIVEN TO BEGIN LAVAGE. 5 ML HAD BEEN ADMINISTERED BEFORE PROCEDURE STOPPED DUE TO PATIENT COUGHING. CHEST X-RAY CONFIRMED TUBE WAS IN BRONCHUS. TUBE PLACEMENT CORRECTED. NO INJURY TO PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BARD NG TUBE NG TUBE FEG C. R. BARD INC UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR