GE Healthcare, LLC: Medical Device Recall in 2020 - (Recall #: Z-1711-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer

Product Classification:

Class II

Date Initiated: December 3, 2019

Date Posted: May 6, 2020

Recall Number: Z-1711-2020

Event ID: 85466

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.

Status: Ongoing

Product Quantity: 123 in total

Code Information:

all affected systems

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

FDA Mandated