--- title: "GE Medical Systems, LLC Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search GE Medical Systems, LLC recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/ge-medical-systems-llc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # GE Medical Systems, LLC recall records **124** reported ongoing 124 records in this archive. Latest source date Jun 5, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Jun 5, 2026 FDA device enforcement ### [Optima XR200amx, Mobile Digital-Ready Radiographic System](https://isitonrecall.com/recall/fda-device-z-2726-2026-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 counterpo... Class II Reported ongoing Distribution: Worldwide - US Nationwide and the countries of Brazil, Canada, Korea, Mexico, Saudi Arabia, Spain, UK. [Official source for Optima XR200amx, Mobile Digital-Ready Radiographic System](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2726-2026%22) Jun 5, 2026 FDA device enforcement ### [Optima XR220amx, Mobile Digital-Ready Radiographic System](https://isitonrecall.com/recall/fda-device-z-2727-2026-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 counterpo... Class II Reported ongoing Distribution: Worldwide - US Nationwide and the countries of Brazil, Canada, Korea, Mexico, Saudi Arabia, Spain, UK. [Official source for Optima XR220amx, Mobile Digital-Ready Radiographic System](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2727-2026%22) Jun 5, 2026 FDA device enforcement ### [Optima XR240amx, Mobile Digital Radiographic System](https://isitonrecall.com/recall/fda-device-z-2728-2026-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 counterpo... Class II Reported ongoing Distribution: Worldwide - US Nationwide and the countries of Brazil, Canada, Korea, Mexico, Saudi Arabia, Spain, UK. [Official source for Optima XR240amx, Mobile Digital Radiographic System](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2728-2026%22) May 1, 2026 FDA device enforcement ### [Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All Models](https://isitonrecall.com/recall/fda-device-z-2475-2026-giraffe-omnibed-a-combination-of-an-infant-incubator-and-an-infant-warmer-all-models/) 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. I... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All Models](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2475-2026%22) May 1, 2026 FDA device enforcement ### [Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1, a combination of an infant incubator and an infant warmer, Model Numbers 2082844-001-XXX](https://isitonrecall.com/recall/fda-device-z-2476-2026-giraffe-omnibed-carestations-and-giraffe-omnibed-carestation-cs1-a-combination-of-an-infant-incubato/) 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. I... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1, a combination of an infant incu...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2476-2026%22) May 1, 2026 FDA device enforcement ### [Giraffe OmniBed Field Replaceable Unit (FRU), Model Numbers 6600-1056-400 and 6600-1461-500](https://isitonrecall.com/recall/fda-device-z-2477-2026-giraffe-omnibed-field-replaceable-unit-fru-model-numbers-6600-1056-400-and-6600-1461-500/) 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. I... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Giraffe OmniBed Field Replaceable Unit (FRU), Model Numbers 6600-1056-400 and 6600-1461-500](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2477-2026%22) Apr 20, 2026 FDA device enforcement ### [Allia IGS 3 Pulse angiographic X-ray system](https://isitonrecall.com/recall/fda-device-z-2314-2026-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 trouble... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Allia IGS 3 Pulse angiographic X-ray system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2314-2026%22) Apr 20, 2026 FDA device enforcement ### [Allia IGS 5 Pulse angiographic X-ray system](https://isitonrecall.com/recall/fda-device-z-2315-2026-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 trouble... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Allia IGS 5 Pulse angiographic X-ray system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2315-2026%22) Apr 20, 2026 FDA device enforcement ### [Allia IGS 7 Pulse angiographic X-ray system](https://isitonrecall.com/recall/fda-device-z-2316-2026-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 trouble... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Allia IGS 7 Pulse angiographic X-ray system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2316-2026%22) Apr 20, 2026 FDA device enforcement ### [Allia IGS Pulse angiographic X-ray system](https://isitonrecall.com/recall/fda-device-z-2317-2026-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 trouble... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Allia IGS Pulse angiographic X-ray system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2317-2026%22) Apr 20, 2026 FDA device enforcement ### [Allia Moveo angiographic X-ray system](https://isitonrecall.com/recall/fda-device-z-2318-2026-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 trouble... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Allia Moveo angiographic X-ray system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2318-2026%22) Mar 26, 2026 FDA device enforcement ### [Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300](https://isitonrecall.com/recall/fda-device-z-2149-2026-revolution-ascend-computed-tomography-model-numbers-6969000-100-and-6969000-300/) 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. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2149-2026%22) Mar 26, 2026 FDA device enforcement ### [Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6](https://isitonrecall.com/recall/fda-device-z-2150-2026-revolution-ct-x-ray-computed-tomography-model-numbers-5590000-and-5590000-6/) 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. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2150-2026%22) Mar 26, 2026 FDA device enforcement ### [Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23](https://isitonrecall.com/recall/fda-device-z-2151-2026-revolution-apex-elite-x-ray-computed-tomography-model-number-5590000-23/) 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. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2151-2026%22) Mar 26, 2026 FDA device enforcement ### [Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25](https://isitonrecall.com/recall/fda-device-z-2152-2026-revolution-apex-plus-x-ray-computed-tomography-model-number-5590000-25/) 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. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2152-2026%22) Mar 26, 2026 FDA device enforcement ### [Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15](https://isitonrecall.com/recall/fda-device-z-2153-2026-revolution-ct-es-x-ray-computed-tomography-model-number-5590000-15/) 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. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2153-2026%22) Mar 26, 2026 FDA device enforcement ### [Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20](https://isitonrecall.com/recall/fda-device-z-2154-2026-revolution-apex-x-ray-computed-tomography-model-number-5590000-20/) 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. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2154-2026%22) Mar 26, 2026 FDA device enforcement ### [Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27](https://isitonrecall.com/recall/fda-device-z-2155-2026-revolution-apex-select-x-ray-computed-tomography-model-number-5590000-27/) 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. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2155-2026%22) Feb 3, 2026 FDA device enforcement ### [Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LP](https://isitonrecall.com/recall/fda-device-z-1590-2026-imactis-ct-navigation-system-stereotaxic-accessory-for-computer-tomography-ct-systems-model-numbers/) There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide. [Official source for Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1590-2026%22) Jan 30, 2026 FDA device enforcement ### [Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model ...](https://isitonrecall.com/recall/fda-device-z-1569-2026-centricity-universal-viewer-software-versions-7-0-through-7-0-sp2-0-1-a-device-that-displays-medical/) 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 avai... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays med...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1569-2026%22) ## Reasons in these listed records - 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, th... - 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 fas... - 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 ... - 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. These examples come from this result page and are not a ranking of every recall reason. ## Checking GE Medical Systems, LLC ### Is there a recall on ge medical systems, llc right now? This archive contains 124 records, including 124 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search GE Medical Systems, LLC](https://isitonrecall.com/check/?q=GE%20Medical%20Systems%2C%20LLC) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)