Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MRIdian Linac Radiation Therapy System Model 10000 and 20000 Recalled by Viewray, Inc. Due to Issue with transferring treatment regiment from one system...
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 Viewray, Inc. directly.
Affected Products
MRIdian Linac Radiation Therapy System Model 10000 and 20000
Quantity: 24 Systems
Why Was This Recalled?
Issue with transferring treatment regiment from one system to another. Adequate instructions for transferring treatment plan(s) are not provided within the operator's manual or within the software operating system.
Where Was This Sold?
This product was distributed to 7 states: CA, FL, IL, MI, MO, NY, WI
About Viewray, Inc.
Viewray, Inc. has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report