Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ARTIS one with a hybrid cable- An angiography system developed Recalled by Siemens Medical Solutions USA, Inc Due to Examination room monitor connected with the hybrid cable...
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 one with a hybrid cable- An angiography system developed for diagnostic imaging and interventional procedures. Material Number: 10848600
Quantity: 4 units US
Why Was This Recalled?
Examination room monitor connected with the hybrid cable may have a display issue and no image function is available
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