# FDA recall Z-1302-2025

> **GE Medical Systems, LLC** · Class II · device recall initiated 2025-02-18.

## Product

GE Healthcare Revolution CT, System, X-ray, Tomography, Computed

## Reason for recall

GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1302-2025
- **Recalling firm:** GE Medical Systems, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-18
- **Report date:** 2025-03-19

- **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-1302-2025

## Citation

> AI Analytics. FDA recall Z-1302-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1302-2025. Source: US FDA. Licensed CC0.

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