GE Medical Systems, LLC Recalls

22 recalls on record in the United States

medical: 22
medical Class II
2026-04-01

GE Medical Systems, LLC recalls Imactis CT-Navigation System, stereotaxic accessory for Comp

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

View recall details →

medical Class II
2026-03-25

GE Medical Systems, LLC recalls Centricity Universal Viewer Software Versions 6.0 through 6.

There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.

View recall details →

medical Class II
2026-03-25

GE Medical Systems, LLC recalls Centricity Universal Viewer Software Versions 5.0 SP6 throug

There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.

View recall details →

medical Class II
2026-03-25

GE Medical Systems, LLC recalls Centricity Universal Viewer Software Versions 7.0 through 7.

There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.

View recall details →

medical Class II
2026-05-20

GE Medical Systems, LLC recalls Revolution CT ES, X-ray Computed Tomography, Model Number 55

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.

View recall details →

medical Class II
2026-05-20

GE Medical Systems, LLC recalls Revolution Ascend, computed tomography, Model Numbers 696900

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.

View recall details →

medical Class II
2026-05-20

GE Medical Systems, LLC recalls Revolution Apex Select, X-ray Computed Tomography, Model Num

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.

View recall details →

medical Class II
2026-05-20

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

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.

View recall details →

medical Class II
2026-05-20

GE Medical Systems, LLC recalls Revolution Apex, X-ray Computed Tomography, Model Number 559

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.

View recall details →

medical Class II
2026-05-20

GE Medical Systems, LLC recalls Revolution Apex Plus, X-ray Computed Tomography, Model Numbe

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.

View recall details →

medical Class II
2026-05-20

GE Medical Systems, LLC recalls Revolution CT, x-ray computed tomography, Model Numbers 5590

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.

View recall details →

medical Class II
2026-06-17

GE Medical Systems, LLC recalls Allia IGS 3 Pulse angiographic X-ray system

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.

View recall details →

medical Class II
2026-06-17

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

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.

View recall details →

medical Class II
2026-06-17

GE Medical Systems, LLC recalls Allia Moveo angiographic X-ray system

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.

View recall details →

medical Class II
2026-06-17

GE Medical Systems, LLC recalls Allia IGS 5 Pulse angiographic X-ray system

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.

View recall details →

medical Class II
2026-06-17

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

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.

View recall details →

medical Class II
2026-06-24

GE Medical Systems, LLC recalls Giraffe OmniBed Field Replaceable Unit (FRU), Model Numbers

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

View recall details →

medical Class II
2026-06-24

GE Medical Systems, LLC recalls Giraffe OmniBed, a combination of an infant incubator and an

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

View recall details →

medical Class II
2026-06-24

GE Medical Systems, LLC recalls Giraffe OmniBed Carestations and Giraffe OmniBed Carestation

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

View recall details →

medical Class II
2026-07-22

GE Medical Systems, LLC recalls Optima XR200amx, Mobile Digital-Ready Radiographic System

GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been performed to confirm proper assembly. If a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work, causing the arm with X-ray tube and collimator to drop downward on the column track. This could result in patient injury during an exam.

View recall details →

medical Class II
2026-07-22

GE Medical Systems, LLC recalls Optima XR220amx, Mobile Digital-Ready Radiographic System

GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been performed to confirm proper assembly. If a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work, causing the arm with X-ray tube and collimator to drop downward on the column track. This could result in patient injury during an exam.

View recall details →

medical Class II
2026-07-22

GE Medical Systems, LLC recalls Optima XR240amx, Mobile Digital Radiographic System

GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been performed to confirm proper assembly. If a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work, causing the arm with X-ray tube and collimator to drop downward on the column track. This could result in patient injury during an exam.

View recall details →