Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 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 Max -fluoroscopic X-ray system Model # 10762473 Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
Quantity: 191
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