BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ENDOTRACHEAL TUBE, 7.5

    MDR report key: 15714 · Received September 1, 1994

    Report

    Report Number
    MW1003243
    Event Type
    Injury
    Date Received
    September 1, 1994
    Date of Event
    August 16, 1994
    Report Date
    August 17, 1994
    Manufacturer
    SHERIDAN CATHETER CORP.
    Product Code
    BTR
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    RESPIRATORY THERAPIST

    Narratives

    Description of Event or Problem · 1

    WHILE PT BEING SUCTIONED, CUFF ON ENDOTRACHEAL TUBE DEFLATED, RESPIRATORY THERAPY ATTEMPTED TO INFLATE CUFF WITHOUT SUCCESS. PT BAGGED, ER PHYSICIAN CALLED AND PT REINTUBATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ENDOTRACHEAL TUBE, 7.5 BTR SHERIDAN CATHETER CORP. 018535

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Life Threatening MECHANICAL VENTILATOR 8/15/94 THROUGH PRESENT