FDAApril 9, 2019device

Artis Q (material 10848280, 10848281, 10848282) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that...

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

The hazard

In affected Artis systems the movement of the floating tabletop may be blocked after a collision sensor has been activated during system movement.

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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