FDA Adverse Event Malfunction Summary report: N

GEMINI TF 64 SLICE PET/CT SYSTEM

MDR report key: 920286 · Received September 26, 2007

Report

Report Number
1525965-2007-00019
Event Type
Malfunction
Date Received
September 26, 2007
Date of Event
May 30, 2007
Report Date
September 26, 2007
Manufacturer
PHILIPS MEDICAL SYSTEMS, INC.
Product Code
KPS
PMA / PMN Number
K052640
Removal / Correction Number
1525965-09/25/07-007C
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THIS MDR IS BEING FILED TO ADD ADDITIONAL PRODUCT CONFIGURATIONS TO AN MDR PREVIOUSLY FILED ON THE BRILLIANCE EBW WORKSTATION CARDIAC VIEWER (REFERENCE MDR 1525965-2007-00005). ADDITIONAL INVESTIGATION HAS DETERMINED THAT THE ISSUE IMPACTS THE CT SUBSYSTEM OF THE GEMINI TF PET/CT SYSTEMS AS WELL. NO OCCURRENCES OF THIS EVENT HAVE BEEN REPORTED ON GEMINI TF SYSTEMS IN THE FIELD. PLEASE REFERENCE THE ABOVE MENTIONED C&R REPORT FOR ADDITIONAL INFORMATION.

Description of Event or Problem · 1

THE EXTENDED BRILLIANCE WORKSPACE (EBW) HAS AN OPTIONAL SOFTWARE APPLICATION FUNCTION CALLED THE CARDIAC VIEWER. IT IS POSSIBLE FOR AN SET OF IMAGES TO BE EXPANDED OR ZOOMED AND SAVED AS A NEW SET OF IMAGES. WHEN THE SAVED SET OF IMAGES ARE VIEWED USING A FUNCTION CALLED THE CT VIEWER, OR ARE TRANSFERRED TO A PACS (PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM), MEASUREMENTS MADE ON THESE ZOOMED IMAGES ARE INCORRECT. THE MEASUREMENT ERROR IS PROPORTIONAL TO THE ZOOM FACTOR. AN IMAGE WHICH IS ZOOMED BY A FACTOR OF TWO WILL SHOW DISTANCE MEASUREMENTS THAT ARE INCORRECT AND ENLARGED BY A FACTOR OF TWO.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GEMINI TF 64 SLICE PET/CT SYSTEM GEMINI TF 64 KPS PHILIPS MEDICAL SYSTEMS, INC. 4535 679 94741

Patients

Seq Age Sex Outcome Treatment
1 NA YR