Class II

Medical Device Recall: UROSKOP Omnia Max. Model Number: 10762473

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

25 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1982-2025

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.