FDAClass IIMay 20, 2026

Revolution Apex Plus recall

Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25

Why was Revolution Apex Plus recalled?

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.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI-DI: 00195278502179; Serial Numbers: REV282400012CN REV282400006CN REV282400038CN REV282400011CN REV282400003CN REV282400013CN REV282300006CN REV282400021CN REV282300013CN REV282400035CN REV282300022CN

Product
Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25
Recalling firm
GE Medical Systems, LLC
Quantity
11 units
Distribution
Worldwide - US Nationwide distribution.
Recall date
May 20, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls