FDAMay 24, 2022device

Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System

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

The hazard

It may occur that after system startup no stand movement is possible any longer in the event of a discharged BIOS battery of the robotic stand control PC. If this problem occurs during startup, all stand movements are blocked and can only be reactivated by a field service engineer.

What to do

FDA enforcement status: Terminated

Brands named

siemens medical solutionssiemenssiemens medical

UPCs

0405686901008304056869010007

Recall history

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

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