CLASS II ONGOING Device recall · Reported 20 May 2026 · FDA Enforcement Report

Revolution CT ES, X-ray Computed Tomography recalled

GE Medical Systems is recalling Revolution CT ES, X-ray Computed Tomography, distributed nationwide in the US. The recall was initiated on 26 Mar 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI-DI: 00840682123471; Serial Numbers: REVV82200058CN REVV82200046CN REVV82100016CN REVV82200014CN REVV82100027CN REVV82200047CN REVV82100031CN REVV82400010CN REVV82200017CN REVV82400005CN

Quantity recalled10 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2153-2026
FDA event ID: 98738
Recalling firm: GE Medical Systems, Waukesha, WI
Classification: Class II
Status: Ongoing
Recall initiated: 26 Mar 2026
FDA classified: 8 May 2026
Reported: 20 May 2026
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Imaging Equipment

Timeline

26 Mar 2026	Recall initiated by company
8 May 2026	Classified by FDA	+43 days
20 May 2026	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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 as listed by the FDA

Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15

Where it was distributed

Worldwide - US Nationwide distribution.

Nationwide

Questions about this recall

Is Revolution CT ES, X-ray Computed Tomography recalled?

Yes. GE Medical Systems recalled Revolution CT ES, X-ray Computed Tomography on 26 Mar 2026. The recall is Class II and its status is Ongoing. Recall number Z-2153-2026.

Why was it recalled?

Which lots are affected?

UDI-DI: 00840682123471; Serial Numbers: REVV82200058CN REVV82200046CN REVV82100016CN REVV82200014CN REVV82100027CN REVV82200047CN REVV82100031CN REVV82400010CN REVV82200017CN REVV82400005CN

Where was it sold?

Worldwide - US Nationwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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