Ge Healthcare DPX-NT series, GE Lunar DEXA bone densitometers operating with enCORE software versions 12.0, 12.1, 12.2,13.0, & 13.1. The systems provide an estimate of BMD. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DPX-NT series, GE Lunar DEXA bone densitometers operating with enCORE software versions 12.0, 12.1, 12.2,13.0, & 13.1. The systems provide an estimate of BMD.
Brand
Ge Healthcare
Lot Codes / Batch Numbers
software versions 12.0, 12.1, 12.2, 13.0, & 13.1.
Products Sold
software versions 12.0, 12.1, 12.2,13.0, & 13.1.
Ge Healthcare is recalling DPX-NT series, GE Lunar DEXA bone densitometers operating with enCORE software versions 12.0, 12.1, due to Failure to properly pre-indicate the technique factors to be used during a patient scan.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Failure to properly pre-indicate the technique factors to be used during a patient scan.
Recommended Action
Per FDA guidance
An Important Electronic Product Radiation Warning letter will be sent to customers. The letter will discuss the defect description and related hazards, the affected product details, safety instructions, and product correction. Customers are to contact their local GE Healthcare service representative with questions.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026