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GE Healthcare, LLC recalls Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer
Recalled May 6, 2020 · FDA recall Z-1712-2020 · GE Healthcare
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. · FDA Class II
Units
123 in total
Sold at
US Nationwide Distribution
Description
An issue with the Lunar iDXA control panel may cause the start button to not release and potentially contribute to an accidental radiation occurrence.
Product
Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer
Manufacturer(s)
GE Healthcare, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →