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Siemens Medical Solutions USA, Inc recalls UROSKOP Omnia. Model Number: 10094910
Recalled June 25, 2025 · FDA recall Z-1981-2025 · Siemens Medical Solutions USA
Hazard
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire. · FDA Class II
Units
95 units
Sold at
Nationwide distribution.
Description
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
Product
UROSKOP Omnia. Model Number: 10094910
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →