FDAMarch 26, 2021device

Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number: 10094137

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

The hazard

Some Artis zee ceiling systems show an increased abrasion of the cabling at the cable outlet of the inner C-arm, the limited functionality may not be sufficient to continue with treatment as planned. This may result in a situation where it is necessary to cancel clinical treatment or to continue treatment on an alternative system.

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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Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number: 10094137 — Recall Details · AllClear