Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Artis systems with large display from Siemens Medical Solutions USA Recalled by Siemens Medical Solutions USA, Inc Due to Due to improper soldering in a limited number...
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 systems with large display from Siemens Medical Solutions USA, Inc. Interventional Fluoroscopic X-ray for angiographic procedures.
Quantity: 17
Why Was This Recalled?
Due to improper soldering in a limited number of large display bypass module components of a specific production lot, a loss of video signal could potentially occur. This has not been observed in the field and only sporadic cases have been observed in factory screening.
Where Was This Sold?
This product was distributed to 12 states: AL, CA, FL, IL, MA, MI, NJ, ND, OH, TN, TX, WI
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