FDAFebruary 27, 2017device

Artis Q and Q.Zen fluoroscopic x-ray system

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

The hazard

A gap in the housing of the wireless foot switch could potentially result in liquids penetrating the interior. Such liquids may include disinfectants, cleaning agents and/ or bodily fluids. In rare cases, the introduction of liquids in the wireless foot switch housing could result in the failure of the foot switch.

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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Artis Q and Q.Zen fluoroscopic x-ray system — Recall Details · AllClear