FDAFDA · Food and drugs·Recall number Z-1709-2020
Lunar iDXA bone densitometer
Published May 6, 2020 · Recall initiated: December 3, 2019
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the 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.
What to do
FDA Mandated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- GE Healthcare, LLC
- Distributor
- US Nationwide Distribution
- Lot
- all affected systems
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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