FDA Adverse Event Injury Summary report: N

PHILIPS MEDICAL SYSTEMS CLINIX MP PLUS

MDR report key: 672208 · Received February 6, 2006

Report

Report Number
1525965-2006-00001
Event Type
Injury
Date Received
February 6, 2006
Date of Event
January 30, 2006
Report Date
February 6, 2006
Manufacturer
PHILIPS MEDICAL SYSTEMS
Product Code
IZL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE SYSTEM CONSISTS OF A PT TABLE, A STATIONARY L-ARM AND A MOVABLE C-ARM GANTRY. A NURSE WAS BEHIND THE PT TABLE MOVING THE PT AND SHE WAS STANDING IN AN AREA WHICH IS IDENTIFIED AND LABELED AS A POTENTIAL CRUSH POINT. THE ROOM LIGHTS WERE TURNED DOWN. THE DOCTOR MOVED THE C-ARM GANTRY TO THE FOOT END AND TRAPPED THE NURSE BETWEEN THE C-ARM GANTRY AND THE STATIONARY L-ARM. THE NURSE SUSTAINED BILATERAL CLAVICLE FRACTURES AND WAS ADMITTED TO THE HOSP AFTER THE EVENT. THE PT ON THE TABLE WAS NOT INVOLVED IN THE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PHILIPS MEDICAL SYSTEMS CLINIX MP PLUS X-RAY SYSTEM WITH MOVABLE C-ARM IZL PHILIPS MEDICAL SYSTEMS 356920 NA

Patients

Seq Age Sex Outcome Treatment
1 NA Hospitalization