# FDA recall Z-2590-2021

> **GE Healthcare, LLC** · Class II · device recall initiated 2021-06-24.

## 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.

## Distribution

Domestic Distribution Only

## Key facts

- **Recall number:** Z-2590-2021
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-06-24
- **Report date:** 2021-10-06
- **Termination date:** 2023-06-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2590-2021

## Citation

> AI Analytics. FDA recall Z-2590-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2590-2021. Source: US FDA. Licensed CC0.

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