FDA Adverse Event Injury Summary report: N

HEATED WITH BREATHING CIRCUIT

MDR report key: 1192643 · Received October 10, 2008

Report

Report Number
1192643
Event Type
Injury
Date Received
October 10, 2008
Date of Event
August 25, 2008
Report Date
October 10, 2008
Manufacturer
WESTMED, INC.
Product Code
CAI
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Location
FL, US

Narratives

Description of Event or Problem · 1

I WAS FINISHING THE DRAPING OF MY PATIENT FOR EPS PROCEDURE, I HEARD A MUFFLED POP AND OBSERVERD THE ANESTHESIA CIRCUIT IN FLAME. I IMMEDIATELY PUSHED THE CIRCUIT AWAY FROM THE PATIENT,THE FLAME WAS EXTINGUISHED AND STOMPED OUT ON THE FLOOR, PT WAS NOT CONNECTED TO CIRCUIT, WAS ON NASAL CANNULA OXYGEN. OXYGEN WAS BEING RUN THROUGH CIRCUIT . NO HARM TO PT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HEATED WITH BREATHING CIRCUIT NASAL CANNULA CAI WESTMED, INC. 200 *

Patients

Seq Age Sex Outcome Treatment
1 74 YR Required Intervention