← FDA ENFORCEMENT
Z-2154-2026Class II

GE Medical Systems, LLC

Recalling firm
GE Medical Systems, LLC
Product type
Device
Status
Ongoing
Report date
2026-05-20
Distribution
Worldwide - US Nationwide distribution.
Firm state
WI
Product quantity
24 units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Data Integrity
Reason for recall

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.

Product description

Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20

Code / lot info

UDI-DI: 00840682146616; Serial Numbers: REV2A2200014CN REV2A2200072CN REV2A2100016CN REV2A2200068CN REV2A2200034CN REV2A2200116CN REV2A2200037CN REV2A2000006CN REV2A2200041CN REV2A2100011CN REV2A2100048CN REV2A2200015CN REV2A2100038CN REV2A2200011CN REV242200002CN REV2A2200120CN REV2A2200018CN REV2A2300016CN REV2A2200067CN REV2A2000007CN REV2A2200105CN REV2A2200007CN REV2A2000032CN REV2A2100019CN

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.