Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1302-2025 — GE Healthcare Revolution CT, System, X-ray, Tomography, Computed

U.S. FDA — Device Enforcement · United States · 2025-02-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1302-2025
Date of alert
2025-02-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Medical Systems, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00195278460271
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.