FDA Device recall Z-2590-2021
AMX Navigate Mobile X-Ray System
- FDA Device
- Class II
- terminated
- Published 2021-10-06
On 2021-10-06 the FDA classified a Class II recall of AMX Navigate Mobile X-Ray System by Ge Healthcare, citing an unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2590-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-06-24 |
| Published | 2021-10-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Ge Healthcare |
| Distribution | n/a |
Product
AMX Navigate Mobile X-Ray System
Reason
An unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system.
Identifiers
| code_info | AMXNV2000001WK, AMXNV2000002WK, DF2401600003WK |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2590-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.