FDADecember 23, 2015device

GE Healthcare, Optima XR220amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.

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

The hazard

Potential safety latch mechanism failure. The safety latch, within the column that supports the horizontal arm, is a backup in the unlikely event the primary safety cable breaks. A fall of the arm assembly could result in bodily harm to a person.

What to do

FDA enforcement status: Terminated

Brands named

ge medical systems

UPCs

00000076835

Recall history

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

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