FDAMay 1, 2018device

Artis Q.zen floor, Material no. 10848353, for angiography and whole body radiographic/fluoroscopic procedures.

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

The hazard

After the Large Display returns from power save mode, it may not show an image, and stay black without showing an error message although X-ray is still possible. The problem does not occur during an ongoing procedure. If the problem occurs, the system cannot be operated normally. It may be necessary to cancel or restart the treatment or transfer the patient to an alternate or another system.

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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