Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Artis Zee Angiographic x-ray systems. Recalled by Siemens Medical Solutions USA, Inc Due to An inappropriate cable connection was assembled for certain...
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 Zee Angiographic x-ray systems.
Quantity: 9
Why Was This Recalled?
An inappropriate cable connection was assembled for certain Artis zee systems. which may cause a system failure and possibly lead to a restricted maneuverability of the gantry system.
Where Was This Sold?
This product was distributed to 9 states: AL, AR, MI, MN, NJ, NC, OH, PA, 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