Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Artis zee/ zeego Interventional Fluoroscopic X-Ray System Recalled by Siemens Medical Solutions USA, Inc Due to In affected Artis zee floor Interventional Fluoroscopic X-Ray...
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/ zeego Interventional Fluoroscopic X-Ray System, Model Number: 10094142, Software Version: VC21C
Quantity: 3
Why Was This Recalled?
In affected Artis zee floor Interventional Fluoroscopic X-Ray Systems, the activation of a collision sensor will cause a block the movement of the floating tabletop and could result in a delay or interruption of a procedure.
Where Was This Sold?
This product was distributed to 2 states: TX, WA
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