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FDAFebruary 23, 2017device

Ziehm Imaging solo FD Mobile Fluoroscopic C-arm

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

The hazard

During Ziehm Imaging GmbH FDA inspection, the label for the Collimator and X-ray Control panel was missing the manufacturer date as part of the identification for certified component

What to do

FDA enforcement status: Terminated

Brands named

ziehm imagingziehm

Recall history

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

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