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RecallsAboutBlog

GE Medical Systems, LLC

GE Medical Systems, LLC: 6 recalls listed since March 2026 across FDA.

By year

  • 20266

By agency

  • FDA6

By category

  • Medical Device6

All recalls (6)

GE Optima XR200amx, XR220amx and XR240amx Radiographic Systems

This could result in patient injury during an exam.

Moderate risk, FDA, , Device defect

GE HealthCare Giraffe OmniBed Devices

The Giraffe OmniBed has a potential issue with the canopy soffit that could cause patient injury.

Moderate risk, FDA, , Device defect

Allia Angiographic X-Ray System

The Allia IGS 3 Pulse angiographic X-ray system has an electrical cable issue that could cause electrical shock to service personnel.

Moderate risk, FDA, , Device defect

GE HealthCare Revolution CT Scanners

GE HealthCare computed tomography systems have a potential security vulnerability that could impact AW Server via Edison Health Link.

Moderate risk, FDA, , Software defect

GE Medical Systems Imactis CT-Navigation Systems

There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position.

Moderate risk, FDA, , Device defect

Centricity Universal Viewer Software

Centricity Universal Viewer Software has a cybersecurity vulnerability that may expose user login credentials.

Moderate risk, FDA, , Software defect
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