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

Recall Z-2151-2026 — Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23

U.S. FDA — Device Enforcement · United States · 2026-03-26 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2151-2026
Date of alert
2026-03-26
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 security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
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.

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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.