FDA Adverse Event Injury Summary report: N

G.E. MED SYSTEMS

MDR report key: 231263 · Received June 30, 1999

Report

Report Number
MW1016706
Event Type
Injury
Date Received
June 30, 1999
Date of Event
June 21, 1999
Report Date
June 29, 1999
Manufacturer
GENERAL ELECTRIC MEDICAL SYSTEMS
Product Code
JAK
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
AZ, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

51 YEAR OLD FEMALE PLACED ON CT TABLE FOR SCAN. AS TABLE WAS FEEDING INTO MACHINE, TABLE BEGAN TO TILT. PT IN DANGER OF FALLING TO FLOOR ON HER HEAD. ATTENDANT GRABBED TABLE AND PREVENTED PT FROM FALLING TO FLOOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 G.E. MED SYSTEMS LXI CI SCANNER PATIENT TABLE JAK GENERAL ELECTRIC MEDICAL SYSTEMS * *

Patients

Seq Age Sex Outcome Treatment
1 51 YR Required Intervention