FDA Adverse Event Summary report: N

EMERSON HEATING LAMP

MDR report key: 3220840 · Received July 1, 2013

Report

Report Number
3220840
Date Received
July 1, 2013
Date of Event
June 14, 2013
Report Date
June 24, 2013
Manufacturer
PHILIPS RESPIRONICS (FORMERLY J.H. EMERSON CO.)
Product Code
ILY
Report Source
User Facility report
Reporter Location
CA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PREEMIE UNDERWENT SURGERY FOR REPAIR OF GASTROSCHISIS. AFTER SURGERY, IT WAS NOTED,THAT INFANT WAS HYPOTHERMIC. WARMING MEASURES WERE INITIATED WHICH INCLUDED HEATING LAMP. THE INFANT WAS PLACED APPROXIMATELY 2.5-3 FEET AWAY FROM THE HEATING LAMP. AFTER RETURNING FROM THE OPERATING ROOM, ERYTHEMATOUS REGION WAS NOTED ON THE RIGHT CHEST BELOW THE CLAVICLE.WHAT WAS THE ORIGINAL INTENDED PROCEDURE?WARMING MEASURESDEVICE #1IS THIS A LABORATORY DEVICE OR LABORATORY TEST?NO

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
297268 EMERSON HEATING LAMP LAMP, INFRARED, THERAPEUTIC HEATING ILY PHILIPS RESPIRONICS (FORMERLY J.H. EMERSON CO.) 96HB *

Patients

Seq Age Sex Outcome Treatment
1 1 DAY