Unrated Medical device recall · FDA · Published March 26, 2026

GE Revolution CT ES Security Vulnerability Recall: Potential Data Exposure

GE Medical Systems recalls Revolution CT ES X-ray CT scanners with model 5590000-15 due to a security vulnerability in the AW Server that could expose patient data. Affected units include specific serial numbers listed in the recall notice.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2153-2026Medical device GE Medical Systems ›

Recall notice

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.

Take action

Contact the company

Recalling firmGE Medical Systems, LLC3000 N Grandview Blvd · Waukesha, WI 53188-1615

✎ GovInfoNow plain-language explainer

GE Medical Systems is recalling Revolution CT ES X-ray CT scanners with model number 5590000-15 because of a security vulnerability in the AW Server. This could allow unauthorized access to patient data if the system is connected to certain networks. Read more at govinfonow.com/recall/49588-ge-revolution-ct-es-security-vulnerability-recall-potential-data-exposure.

Source Summary by GovInfoNow · govinfonow.com/recall/49588-ge-revolution-ct-es-security-vulnerability-recall-potential-data-exposure · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2153-2026

Cite this page

“GE Revolution CT ES Security Vulnerability Recall: Potential Data Exposure.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/49588-ge-revolution-ct-es-security-vulnerability-recall-potential-data-exposure. Based on FDA recall #Z-2153-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2153-2026%22&limit=1).

GE Medical Systems, LLC recalled Revolution CT ES X-ray Computed Tomography units due to a potential security vulnerability, according to the FDA on March 26, 2026.

How to tell if you have it

Brand: GE Medical Systems
Product: Revolution CT ES, X-ray Computed Tomography
Model Number: 5590000-15
UDI-DI: 00840682123471
Serial Numbers: REVV82200058CN, REVV82200046CN, REVV82100016CN, REVV82200014CN, REVV82100027CN, REVV82200047CN, REVV82100031CN, REVV82400010CN, REVV82200017CN, REVV82400005CN

The hazard

The recall addresses 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.

Context

GovInfoNow's records show GE Medical Systems, LLC has had 27 other recalls since March 30, 2018. Recent brand recalls include a column safety failure risk for the Optima XR240amx Mobile X-Ray System on June 5, 2026, and a patient injury risk from a loose canopy soffit for the Giraffe OmniBed FRU on May 1, 2026. Other recent recalls of similar products include a GE Healthcare patient monitor software vulnerability on July 10, 2026, and Edan Diagnostics patient monitor cybersecurity risks on October 24, 2025.

How to tell if you have this one

Check for the model number 5590000-15 on the scanner. Affected units have specific serial numbers listed in the recall notice, including REVV82200058CN and others.

Brand
GE Medical Systems
Category
Medical device

FDA recall event · 7 products

All 7 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
Worldwide - US Nationwide distribution.

Recall number	Product, codes & lots	Quantity
Z-2149-2026	Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300; UDI-DI: 00840682146173; Serial Numbers: AS10G2200136YC AS10G2200101YC AS10G2200068YC AS10G2200035YC AS10G2300093YC AS10G2400094YC AS10G2400079YC AS10G2100008YC AS10G2500002YC CBDWG2400019HM CBDWG2300081HM AS10G2400056YC AS10G2400081YC AS10G2400087YC CBDWG2400117HM CBDWG2400085HM CBDWG2500003HM CBDWG2400140HM CBDWG2400126HM AS10G2200085YC AS10G2300057YC CBDWG2500011HM CBDWG2300056HM CBDWG2300041HM AS10G2300041YC	25 units
Z-2150-2026	Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6; UDI-DI: 00840682118552; Serial Numbers:REVVX2300007CN 443327CN2 REVVX1600034CN REVVX2400004CN REVVX2200047CN 441716CN8 00000440713CN6 REVVX1800043CN 441839CN8 REVVX1700067CN REVVX1800007CN REVVX1800105CN REVVX1800048CN REVVX1900123CN REVVX1800046CN REVVX2000005CN REVVX2200009CN REVVX1600013CN REVVX1700101CN REVVX2200025CN REVVX2100028CN REVVX1900069CN REVVX2100020CN REVVX2100014CN REVVX2100050CN REVVX1600052CN 438902CN9 REVVX1900107CN 438369CN1 REVVX1900018CN REVVX1700071CN REVVX1700082CN 442792CN8 REVVX2200007CN REVVX1700104CN REVVX2000056CN REVVX1900086CN REVVX2200039CN	38 units
Z-2151-2026	Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23; UDI-DI: 00195278460271; Serial Numbers: REV2X2400067CN REV2X2400065CN REV2X2400046CN REV2X2400021CN REV2X2400050CN REV2X2400095CN REV2X2400078CN REV2X2300068CN REV2X2400093CN REV2X2400098CN REV2X2300091CN REV2X2300042CN REV2X2300083CN REV2X2300020CN REV2X2400068CN REV2X2400107CN REV2X2300090CN REV2X2300097CN REV2X2300003CN REV2X2400028CN REV2X2400026CN REV2X2300002CN REV2X2400027CN REV2X2400059CN REV2X2300084CN REV2X2400069CN REV2X2400063CN REV2X2400055CN REV2X2300011CN REV2X2300050CN REV2X2400048CN REV2X2300047CN REV2X2400014CN	33 units
Z-2152-2026	Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25; UDI-DI: 00195278502179; Serial Numbers: REV282400012CN REV282400006CN REV282400038CN REV282400011CN REV282400003CN REV282400013CN REV282300006CN REV282400021CN REV282300013CN REV282400035CN REV282300022CN	11 units
Z-2153-2026	Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15; UDI-DI: 00840682123471; Serial Numbers: REVV82200058CN REVV82200046CN REVV82100016CN REVV82200014CN REVV82100027CN REVV82200047CN REVV82100031CN REVV82400010CN REVV82200017CN REVV82400005CN	10 units
Z-2154-2026	Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20; 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	24 units
Z-2155-2026	Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27; UDI-DI: 00195278469700; Serial Numbers: REV242400001CN REV242400004CN REV242300006CN REV242400002CN REV242300004CN	5 units

Based on the official FDA remedy

What to do — step by step

Check for Recalled Model
Verify the model number on your Revolution CT ES scanner to see if it matches 5590000-15.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “Worldwide - US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 55 days after the firm started it.

Mar 26, 2026Firm started the recall
May 8, 2026FDA classified it Class II
May 20, 2026Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/49588-ge-revolution-ct-es-security-vulnerability-recall-potential-data-exposure">GE Revolution CT ES Security Vulnerability Recall: Potential Data Exposure (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2153-2026 (March 26, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2153-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.