Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Pinnacle3 Radiation Therapy Planning (RTP) System Recalled by Philips Medical Systems (Cleveland), Inc. Due to Philips Medical Systems have recently determined that a...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips Medical Systems (Cleveland), Inc. directly.
Affected Products
Pinnacle3 Radiation Therapy Planning (RTP) System, software version 9.0.
Quantity: 1016
Why Was This Recalled?
Philips Medical Systems have recently determined that a software nonconformance can cause incorrect beam geometry. This issue affects Pinnacle3 Radiation Therapy Planning (RTP) System, software version 9.0 manufactured from 09/29/09 to 12/01/2013.
Where Was This Sold?
This product was distributed to 49 states: AL, AK, AZ, AR, CA, CO, CT, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, DC
About Philips Medical Systems (Cleveland), Inc.
Philips Medical Systems (Cleveland), Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report