Lunar iDXA Pro/Lunar iDXA Advance recall
Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer
Why was Lunar iDXA Pro/Lunar iDXA Advance 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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
all affected systems
- Product
- Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer
- Recalling firm
- GE Healthcare, LLC
- Quantity
- 123 in total
- Distribution
- US Nationwide Distribution
- Recall date
- May 6, 2020
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)