FDA Adverse Event Summary report: N

PHILIPS

MDR report key: 1020409 · Received March 13, 2008

Report

Report Number
1020409
Date Received
March 13, 2008
Date of Event
August 4, 2006
Report Date
March 7, 2008
Manufacturer
PHILIPS MEDICAL SYSTEMS
Product Code
LNH
Report Source
User Facility report
Reporter Location
TX, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

TECHNICIANS WERE MOVING THE IV POLE AND APPROACHED THE 5 GAUSS LINE INSIDE THE MRI ROOM. AT THAT TIME, THE IV POLE WAS CAUGHT IN THE MAGNETIC FIELD AND STARTED MOVING TOWARD THE MRI MACHINE. TECHNOLOGIST WAS STRUCK ON THE ARM BY THE POLE AS IT MOVED TOWARDS THE MRI MACHINE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PHILIPS MRI SYSTEM LNH PHILIPS MEDICAL SYSTEMS ACS INTERA *

Patients

Seq Age Sex Outcome Treatment
1 41 YR