# FDA recall Z-0604-2025

> **GE Healthcare (China) Co., Ltd.** · Class II · device recall initiated 2024-11-05.

## Product

GE Healthcare Revolution Advance, Model number 5849504; X-ray/computed tomography systems

## Reason for recall

GE HealthCare has become aware of a potential issue on certain Discovery, Optima, Revolution series CT systems, and certain operator console upgrades that can result in rotated CT images. Particularly with helical, cine, and cardiac (if applicable) scan modes, after the first image of an exam, each subsequent image can be rotated by an increasing amount. The amount of progressive image rotation is dependent on the gantry speed and the duration of the scan. The final image in the exam can be rotated up to a maximum of ~56 degrees. The entire anatomy rotates as a whole by equal degrees, without distortion, and the anatomical positioning and z-axis of the images remains correct. Small degrees of image rotation might not be noticed. If image rotation is noticed and necessitates a rescan of the patient, the same image rotation will reoccur.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-0604-2025
- **Recalling firm:** GE Healthcare (China) Co., Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-11-05
- **Report date:** 2024-12-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Beijing, China

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0604-2025

## Citation

> AI Analytics. FDA recall Z-0604-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0604-2025. Source: US FDA. Licensed CC0.

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