Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Axiom Artis systems. C-arm angiographic x-ray system x-ray Recalled by Siemens Medical Solutions USA, Inc Due to The firm became aware of a potential issue...
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
Axiom Artis systems. C-arm angiographic x-ray system x-ray, angiographic system.
Quantity: 178
Why Was This Recalled?
The firm became aware of a potential issue with Axiom Artis systems installed by a third party installer that may involve incorrect channel nuts being used.
Where Was This Sold?
This product was distributed to 6 states: DE, MD, NJ, PA, VA, DC
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