Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Plan Parameters workspace within Eclipse Treatment Planning System Version 11 Recalled by Varian Medical Systems, Inc. Due to An anomaly has been traced to a software...
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 Varian Medical Systems, Inc. directly.
Affected Products
Plan Parameters workspace within Eclipse Treatment Planning System Version 11 and 13; ARIA Radiation Oncology versions 11 and 13 Acuity, versions 11 and 13. Manufactured by Varian Medical Systems Palo Alto, CA. Used in radiation therapy simulation.
Quantity: 6701
Why Was This Recalled?
An anomaly has been traced to a software deficiency within the Plan Parameters workspace. When a dose relevant parameter is changed and "do no clear MUs and Reference Point dose" is selected, the Monitor units may change.
Where Was This Sold?
Worldwide Distribution.
About Varian Medical Systems, Inc.
Varian Medical Systems, Inc. has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report