Class II
Medical Device Recall: UROSKOP Omnia. Model Number: 10094910
Siemens Medical Solutions USA, Inc · June 4, 2025
Reason for Recall
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
Distribution
Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
95 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1981-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.