FDA Adverse Event Other Summary report: N

APIX PREMIUM MOBILE IMAGING TABLE

MDR report key: 367929 · Received December 19, 2001

Report

Report Number
1720753-2001-00011
Event Type
Other
Date Received
December 19, 2001
Date of Event
November 27, 2001
Report Date
December 18, 2001
Manufacturer
GE OEC MEDICAL SYSTEMS, INC.
Product Code
IXR
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

AS THE TABLE WAS LOWERED IT CAME INTO CONTACT WITH THE SLIP RING OF AN IV POLE. THIS CAUSED THE TABLE TO LIFT OFF THE GROUND AND TILT TOWARDS THE OPERATOR. THE OPERATOR USED THE LEVEL COMMAND TO LEVEL THE TABLETOP. AFTER THE IV POLE WAS REMOVED AND THE TABLE WAS SET BACK ONTO THE FLOOR, THE TABLETOP SHIFTED TO THE LEFT AND THE PATIENT DROPPED TO THE FLOOR. THIS OCCURRED AT THE CONCLUSION OF THE PROCEDURE WHILE THE PT WAS BEING TAKEN FROM THE TABLE. NO REPORT OF PATIENT INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
57523 APIX PREMIUM MOBILE IMAGING TABLE FLOATING IMAGING TABLE IXR GE OEC MEDICAL SYSTEMS, INC. APIX NA

Patients

Seq Age Sex Outcome Treatment
1 * Required Intervention