Medical device recalls Moderate risk

GE Medical Systems, LLC recalls GE Healthcare Revolution CT ES, System, X-ray, Tomography, Computed

Recall date
February 18, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1303-2025
FDA classification
Class II
Brand / firm
GE Medical Systems, LLC
Sold / distributed
Worldwide distribution.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

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