FDAClass IIMay 6, 2020

Lunar iDXA bone densitometer recall

Lunar iDXA bone densitometer

Why was Lunar iDXA bone densitometer 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 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)
Open FDA enforcement record Latest recalls