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FDAMay 19, 2017device

GE Healthcare Discovery NM/CT 670. 670 Pro, 670 ES X-ray system

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

The hazard

It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.

What to do

FDA enforcement status: Terminated

Brands named

ge healthcare

Recall history

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

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