Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ARTIS Q Recalled by Siemens Medical Solutions USA, Inc Due to In Artis systems with A100G generators, a component...
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
ARTIS Q, Interventional Fluroscopic x-ray system
Quantity: 264 distributed worldwide (112 in the U.S.)
Why Was This Recalled?
In Artis systems with A100G generators, a component can be affected by aging which could result in the potential failure of a module in the high-voltage generator.
Where Was This Sold?
Distributed throughout the United States.
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