FDAFebruary 8, 2019device

Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.

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

The hazard

The swivel arm holding the monitors may become dislodged from the carrying arm.

What to do

FDA enforcement status: Terminated

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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