Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Lantis 6.1 Commander Recalled by Siemens Medical Solutions USA, Inc Due to Potentially affected by the Microsoft Windows Remote Desktop...
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 Siemens Medical Solutions USA, Inc directly.
Affected Products
Lantis 6.1 Commander, Model # 5493072 - Product Usage: Lantis Treatstation is to allow the radiation therapist to deliver treatment to the patient using the mevatron and all available accessories. This entails selecting a patient, selecting today s treatment for that patient, setting up and delivering the treatment fields and recording the delivered treatment. Treatstation supports auto sequencing, a process of automatically downloading a group of fields or segments from the verification and record system to the control of the linear accelerator sequentially, without user intervention. In addition, Lantis Treatstation supports intensity modulation, a process of shaping, modifying and moving the beam around a target to maximize the dose at the target and minimize the dose to normal structures.
Quantity: 2
Why Was This Recalled?
Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP) vulnerability
Where Was This Sold?
This product was distributed to 12 states: AL, FL, GA, IL, NJ, NY, NC, OH, OK, PA, WV, WY
About Siemens Medical Solutions USA, Inc
Siemens Medical Solutions USA, Inc has 613 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report