Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer Recalled by GE Healthcare, LLC Due to An issue with the Lunar iDXA control panel...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GE Healthcare, LLC directly.
Affected Products
Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer
Quantity: 123 in total
Why Was This Recalled?
An issue with the Lunar iDXA control panel may cause the start button to not release and potentially contribute to an accidental radiation occurrence.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE Healthcare, LLC
GE Healthcare, LLC has 474 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report