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.

Siemens Medical Solutions USA, Inc Medical Device Recall: UROSKOP Omnia. Model Number: 10094910 | SafeCheck