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FDAApril 11, 2022device

Artis icono floor-angiography systems developed for single and biplane diagnostic imaging and interventional procedures SMN: 11327700

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

The hazard

if the protective earth is interrupted and an additional fault leads to a fault current, the detection of the fault current may not be ensured may cause an electric shock if a person is in contact with metallic parts of the Carm

What to do

FDA enforcement status: Ongoing

Brands named

siemens medical solutionssiemenssiemens medical

UPCs

04056869149325

Recall history

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

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