Lunar iDXA Advance — Class II medical device recall Z-1710-2020
Ongoing recall by GE Healthcare, LLC, reported 2020-05-06, distributed nationwide. An issue with the Lunar iDXA control panel may cause the start button to not release and potentially contribut
| Recall number | Z-1710-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA mandated |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2019-12-03 |
| Classified | 2020-04-24 |
| Reported by FDA | 2020-05-06 |
| Distributed | Nationwide (US) |
| Quantity | 123 in |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1710-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.