Philips Nuclear Medicine, Inc. The Pinnacle3 Radiation Therapy Planning (RTP) system and its associated software; composed of several modules including the core Pinnacle3 functionality, Syntegra (TM), P3IMRT, P3MD and AcQSim3 (TM). The Pinnacle3 RTP system is composed of a Sun UNIX workstation (or UNIX-complaint computer) running the Solaris operating system and software, and a UNIX terminal emulation package on a personal computer, which allows the user to enter patient data into the system, use that data to construct a p Recall
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According to the U.S. Food and Drug Administration (FDA)
Product
The Pinnacle3 Radiation Therapy Planning (RTP) system and its associated software; composed of several modules including the core Pinnacle3 functionality, Syntegra (TM), P3IMRT, P3MD and AcQSim3 (TM). The Pinnacle3 RTP system is composed of a Sun UNIX workstation (or UNIX-complaint computer) running the Solaris operating system and software, and a UNIX terminal emulation package on a personal computer, which allows the user to enter patient data into the system, use that data to construct a p
Brand
Philips Nuclear Medicine, Inc.
Lot Codes / Batch Numbers
Pinnacle3 Version 7.6c Software Kit Model #9200-0652A-ENG, Pinnacle3 Version 8.0d Software Kit Model #9200-0700A-ENG, Pinnacle3 Version 8.0d p 1 Software Kit Model #9200-0700B-ENG, Pinnacle3 Version 8.0h Software Kit Model #9200-0700C-ENG
Products Sold
Pinnacle3 Version 7.6c Software Kit Model #9200-0652A-ENG;Pinnacle3 Version 8.0d Software Kit Model #9200-0700A-ENG;Pinnacle3 Version 8.0d p 1 Software Kit Model #9200-0700B-ENG;Pinnacle3 Version 8.0h Software Kit Model #9200-0700C-ENG
Philips Nuclear Medicine, Inc. is recalling The Pinnacle3 Radiation Therapy Planning (RTP) system and its associated software; composed of seve due to Incorrect Absolute Marking Coordinates when used with PQ-Series scanners due to a software malfunction. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect Absolute Marking Coordinates when used with PQ-Series scanners due to a software malfunction
Recommended Action
Per FDA guidance
All customers will receive an August 21, 2007, Customer Advisory Notification letter notifying them of the issue and the steps required to avoid the issue. Return receipts will be tracked. This is a short-term fix, a long term software fix will be issued shortly by the firm.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MT, NE, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, DC
Page updated: Jan 10, 2026