BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CUFFED ENDOTRACHEAL TUBE

    MDR report key: 32061 · Received April 18, 1996

    Report

    Report Number
    MW1008896
    Event Type
    Malfunction
    Date Received
    April 18, 1996
    Date of Event
    April 1, 1996
    Report Date
    April 8, 1996
    Manufacturer
    SHERIDAN CATHETER CORP.
    Product Code
    BTR
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PLASTIC CONNECTOR WHICH ALLOWS ENDOTRACHEAL TUBE TO ATTACH TO BREATHING CIRCUIT SEPARATES FROM TUBE DESPITE HAVING BEEN TIGHTENED PRIOR TO INTUBATION.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO