BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SHERIDAN/HVT CUFFED MURPHY ENDOTRACHEAL TUBE

    MDR report key: 517716 · Received March 15, 2004

    Report

    Report Number
    MW1031520
    Event Type
    Malfunction
    Date Received
    March 15, 2004
    Date of Event
    March 12, 2004
    Report Date
    March 15, 2004
    Manufacturer
    HUDSON RCE
    Product Code
    BTR
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CO, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT WAS INTUBATED FOR SURGICAL PROCEDURE WHEN PT'S OXYGEN SATURATIONS DROPPED. FIBEROPTIC TUBE INSERTED INTO ETT AND FOUND THE ETT HAD CRIMPED. ETT WAS MANIPULATED, TO RE-OPEN IN AN EFFORT TO KEEP FROM HAVING TO EXTUBATE AND REINTUBATE PT. THIS IS THE 2ND TIME THIS HAS OCCURRED WITH THIS BRAND ETT. LAST WAS REPORTED 12/2003.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SHERIDAN/HVT CUFFED MURPHY ENDOTRACHEAL TUBE ENDOTRACHEAL TUBE BTR HUDSON RCE * *

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR