Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
UROSKOP Omnia Max. Model Number: 10762473 Recalled by Siemens Medical Solutions USA, Inc Due to A resistor in the frequency inverter may strongly...
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. Model Number: 10762473
Quantity: 25 units
Why Was This Recalled?
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
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