Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ARIA Radiation Therapy Management (RTM) VERSIONS 13.6 Recalled by Varian Medical Systems Imaging Laboratory GmbH Due to Software issue for treatment plan and image management...
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 Imaging Laboratory GmbH directly.
Affected Products
ARIA Radiation Therapy Management (RTM) VERSIONS 13.6, 15.1, 15.5, 15.6, 16.0, 16.1
Quantity: 14
Why Was This Recalled?
Software issue for treatment plan and image management application may result in mismatch values which could result in treatment in the wrong location
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Varian Medical Systems Imaging Laboratory GmbH
Varian Medical Systems Imaging Laboratory GmbH has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report