AMX Navigate Mobile X-Ray System — Class II medical device recall Z-2590-2021
Terminated recall by GE Healthcare, LLC, reported 2021-10-06. An unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system.
| Recall number | Z-2590-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2021-06-24 |
| Classified | 2021-09-29 |
| Reported by FDA | 2021-10-06 |
| Terminated | 2023-06-14 |
| Quantity | 3 units |
Product
AMX Navigate Mobile X-Ray System
Reason for recall
An unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system.
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-2590-2021. 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.