Revolution Apex Select CT Scanner Recall Issued by GE Medical Systems
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 5 units of the Revolution Apex Select X-ray Computed Tomography system due to a potential security vulnerability.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on June 2, 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, medical-device.
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 Apex, Revolution Ascend, and Revolution CT systems.
Which Products Are Affected
Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27. UDI-DI: 00195278469700. Serial Numbers: REV242400001CN, REV242400004CN, REV242300006CN, REV242400002CN, REV242300004CN. Five units distributed nationwide in the United States. Recall number Z-2155-2026. Classification: Class II. Ongoing voluntary recall initiated March 26, 2026.
What You Should Do
Consumers should contact the recalling firm GE Medical Systems, LLC at 3000 N Grandview Blvd, Waukesha, WI 53188-1615 for further information regarding the recall.
Why This Matters
The recall addresses a potential security vulnerability in affected CT systems distributed nationwide.
Source
FDA recall number Z-2155-2026 (event ID 98738).
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 (1,025 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to June 2, 2026.
Frequently Asked Questions
Common questions about this FDA recall.