Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop Recalled by Siemens Medical Solutions USA, Inc Due to The swivel arm holding the monitors may become...
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
Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop Omnia is a solid state detector fluoroscopic X-ray system, primarily for urological applications (functional x-ray diagnosis, endourology and minimal invasive urology/surgery).
Quantity: 6
Why Was This Recalled?
The swivel arm holding the monitors may become dislodged from the carrying arm.
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