Z-1710-2020 Class II Ongoing
Recall Details
- Product Type
- Devices
- Report Date
- May 6, 2020
- Initiation Date
- December 3, 2019
- Termination Date
- N/A
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 123 in total
Product Description
Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer
Reason for Recall
An issue with the Lunar iDXA control panel may cause the start button to not release and potentially contribute to an accidental radiation occurrence.
Distribution Pattern
US Nationwide Distribution
Code Information
all affected systems