GE Healthcare AMX Navigate Mobile X-Ray System Recall: Column Motion Hazard
GE Healthcare recalls AMX Navigate Mobile X-Ray Systems with unexpected column motion during parking. Affected models include AMXNV2000001WK, AMXNV2000:002WK, DF2401600003WK. Stop using immediately to prevent potential injury.
Use caution until it’s fixed
An unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system.
Contact the company
What happened, in plain English
GE Healthcare is recalling certain AMX Navigate Mobile X-Ray Systems due to unexpected column motion when attempting to park the column. This hazard could lead to injury if the system moves unexpectedly during use. Read more at govinfonow.com/recall/62308-ge-healthcare-amx-navigate-mobile-x-ray-system-recall-column.
Source Summary by GovInfoNow · govinfonow.com/recall/62308-ge-healthcare-amx-navigate-mobile-x-ray-system-recall-column · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2590-2021
Cite this page
“GE Healthcare AMX Navigate Mobile X-Ray System Recall: Column Motion Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62308-ge-healthcare-amx-navigate-mobile-x-ray-system-recall-column. Based on FDA recall #Z-2590-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2590-2021%22&limit=1).
Why it’s dangerous
The system's column may move unexpectedly when trying to park it, which could cause the system to tip over or shift. This movement might injure patients or staff during medical procedures.
Who’s affected
Healthcare facilities using the recalled AMX Navigate Mobile X-Ray Systems are most at risk. Patients and staff could be injured if the column moves unexpectedly during operation.
How to tell if you have this one
Check for the model numbers AMXNV2000001WK, AMXNV2000002WK, or DF2401600003WK on the system. The recall applies to specific mobile X-ray systems sold by GE Healthcare.
- Brand
GE Healthcare- Category
Medical device
What to do — step by step
Stop Using Immediately
Discontinue use of the affected AMX Navigate Mobile X-Ray Systems to prevent unexpected column motion.
How this recall unfolded
Recall timeline
FDA terminated this recall 2 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2590-2021 (June 24, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2590-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.