Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ViewRay MRIdian Linac System: Model No. 20000 Recalled by Viewray, Inc. Due to There is a potential that components of the...
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
ViewRay MRIdian Linac System: Model No. 20000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60 Hz, Rated Input in Amperes - 210 A, UDI. The MRIdian system and the MRIdian Linac system, with magnetic resonance imaging capabilities, is intended to provide stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body where radiation treatment is indicated.
Quantity: 35 units
Why Was This Recalled?
There is a potential that components of the receive coil can reach elevated temperatures which has the potential to cause a burn injury to the patient or user.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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