FDAJune 4, 2025device

UROSKOP Omnia. Model Number: 10094910

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.

What to do

FDA enforcement status: Ongoing

Brands named

siemens medical solutionssiemenssiemens medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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