Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Siemens has become aware of three potential software...
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 pheno, Interventional fluoroscopic x-ray system, Model No. 10849000
Quantity: 140 US
Why Was This Recalled?
Siemens has become aware of three potential software issues with ARTIS pheno systems with software version VE10B. This may lead to a hazardous situation for patients if treatment cannot be continued on the system and treatment needs to be continued on an alternate system.
Where Was This Sold?
This product was distributed nationwide across all 50 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