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U.S. Department of Health and Human Services

Class 2 Device Recall Precedence SPECT/CT System

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 Class 2 Device Recall Precedence SPECT/CT Systemsee related information
Date Initiated by FirmSeptember 28, 2007
Date PostedFebruary 08, 2008
Recall Status1 Terminated 3 on February 04, 2009
Recall NumberZ-0676-2008
Recall Event ID 45329
510(K)NumberK041218 
Product Classification Pulse Doppler Ultrasonic Imaging System - Product Code KPS
ProductPhilips Medical Systems -- Cardiac Viewer or Pulmonary Viewer software application version 2.0 in use with Precedence SPECT/CT System and all CT EBW workstations using software version 3.5. Philips Nuclear Medicine, Milpitas, CA 95035
Code Information Model Numbers: 2169-3000A/453560250851;  2169-3001A/453560250861;  2169-3002A/453560253551; and  2169-3003A/453560253561
FEI Number 1525965
Recalling Firm/
Manufacturer		 Phillips Nuclear Medicine
540 Alder Dr Bldg 4
Milpitas CA 95035-7443
For Additional Information Contact
408-321-9100
Manufacturer Reason
for Recall		Incorrect Measurement: The firm discovered a software defect in Cardiac and Pulmonary Viewer software application options used in the Precedence CT Sub-System. The defect causes incorrect measurements in derived images which are zoomed and saved in a batch file.
FDA Determined
Cause 2		Software design
ActionA Customer Advisory Notification was mailed to affected consignees on September 28, 2007. The firm informed consignees that incorrect measurement can occur when the Cardiac Viewer or Pulmonary Viewer is used to zoom and save derived images in batch files. The firm provided instructions for operators to prevent incorrect measurements. Phillips is currently investigating methods to correct this issue and will provide updates, free of charge, when they become available. If you have questions concerning this recall, please contact Phillips Medical at 1-800-722-9377, (option5: Diagnostic Imaging, option 5:NM).
Quantity in Commerce19
DistributionWorldwide Distribution --- USA including states of FL, NY, VT, MD, TX, and MO and country of Canada.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = KPS
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