Revolution CT Recall Issued by GE Medical Systems Over Security Vulnerability
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
GE Medical Systems, LLC is recalling 38 units of Revolution CT systems due to a potential security vulnerability in AW Server deployed via Edison Health Link.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on June 3, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
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 CT systems.
Which Products Are Affected
Revolution CT, x-ray computed tomography systems with Model Numbers 5590000 and 5590000-6. A total of 38 units are affected. The recall covers UDI-DI 00840682118552 and specific serial numbers distributed worldwide with US Nationwide distribution.
What You Should Do
Affected facilities should follow guidance from the recalling firm regarding the security vulnerability.
Why This Matters
The Class II recall addresses a potential security vulnerability in medical imaging systems used in healthcare settings across the United States.
Source
FDA recall number Z-2150-2026. Event ID 98738. Recalling firm: GE Medical Systems, LLC, Waukesha, WI.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (915 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to June 3, 2026.
Frequently Asked Questions
Common questions about this FDA recall.