FDADecember 3, 2019device

Lunar iDXA bone densitometer

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

The hazard

An issue with the Lunar iDXA control panel may cause the start button to not release and potentially contribute to an accidental radiation occurrence.

What to do

FDA enforcement status: Ongoing

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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