medical MODERATE Updated 2026-05-20

GE Medical Systems, LLC recalls Revolution Apex Elite, X-ray Computed Tomography, Model Numb

See all recalls from GE Medical Systems, LLC →

Recalled Product

Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 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

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Revolution Apex Elite, X-ray →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

INSPIREMD Inc recalls CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/

2026-06-17 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

BERLIN HEART GMBH recalls EXCOR Pediatric Ventricular Assist Device (VAD) System Blood

2026-06-17 · Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.

Abbott Medical recalls Merlin" Patient Care System (PCS) software Merlin" PCS 3650

2026-06-17 · Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.

GE Medical Systems, LLC recalls Allia IGS 7 Pulse angiographic X-ray system

2026-06-17 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.