FDAMarch 9, 2026device

ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system

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

The hazard

During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-frame acquisitions. Despite the reported x-ray dose showing 0, an actual x-ray dose is applied to the patient.

What to do

FDA enforcement status: Ongoing

Brands named

siemens medical solutionssiemenssiemens medical

UPCs

4056869046877

Recall history

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

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