--- title: "GE Medical Systems Information Technologies Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search GE Medical Systems Information Technologies Inc 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-information-technologies-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # GE Medical Systems Information Technologies Inc recall records **18** reported ongoing 18 records in this archive. Latest source date Jul 30, 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 Jul 30, 2026 FDA device enforcement ### [Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04, 5867474-13 Product code STU CSCS V3 MAI800 Integrated Part Number 5867474-03 Product Code STV](https://isitonrecall.com/recall/fda-device-z-3143-2026-carescape-central-station-cscs-v3-mas800-desktop-part-number-5867474-04-5867474-13-product-code-stu/) Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04, 5867474-13 Product code ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3143-2026%22) Jul 20, 2026 FDA device enforcement ### [PORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209](https://isitonrecall.com/recall/fda-device-z-3036-2026-portrait-core-services-software-v1-1-ref-5700209/) Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or... Class II Reported ongoing Distribution: US: MI, NY and Australia, Czech Republic, Finland, Germany, Italy, Netherlands, Qatar, Saudi Arabia, Switzerland, United Arab Emirates, United Kingdom. [Official source for PORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3036-2026%22) Jul 20, 2026 FDA device enforcement ### [PORTRAIT COMPUTE AND CORE SERVICES V1.2, Ref# 5700592](https://isitonrecall.com/recall/fda-device-z-3037-2026-portrait-compute-and-core-services-v1-2-ref-5700592/) Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or... Class II Reported ongoing Distribution: US: MI, NY and Australia, Czech Republic, Finland, Germany, Italy, Netherlands, Qatar, Saudi Arabia, Switzerland, United Arab Emirates, United Kingdom. [Official source for PORTRAIT COMPUTE AND CORE SERVICES V1.2, Ref# 5700592](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3037-2026%22) Jul 20, 2026 FDA device enforcement ### [PORTRAIT CORE SERVICES SOFTWARE V1.0.5, Ref# 5697353](https://isitonrecall.com/recall/fda-device-z-3038-2026-portrait-core-services-software-v1-0-5-ref-5697353/) Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or... Class II Reported ongoing Distribution: US: MI, NY and Australia, Czech Republic, Finland, Germany, Italy, Netherlands, Qatar, Saudi Arabia, Switzerland, United Arab Emirates, United Kingdom. [Official source for PORTRAIT CORE SERVICES SOFTWARE V1.0.5, Ref# 5697353](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3038-2026%22) Jul 20, 2026 FDA device enforcement ### [FRU (Field replaceable unit), PORTRAIT CORE SERVICES SW RELOAD V1.1, Ref# 5700225](https://isitonrecall.com/recall/fda-device-z-3039-2026-fru-field-replaceable-unit-portrait-core-services-sw-reload-v1-1-ref-5700225/) Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or... Class II Reported ongoing Distribution: US: MI, NY and Australia, Czech Republic, Finland, Germany, Italy, Netherlands, Qatar, Saudi Arabia, Switzerland, United Arab Emirates, United Kingdom. [Official source for FRU (Field replaceable unit), PORTRAIT CORE SERVICES SW RELOAD V1.1, Ref# 5700225](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3039-2026%22) Jul 10, 2026 FDA device enforcement ### [GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system](https://isitonrecall.com/recall/fda-device-z-2878-2026-ge-healthcare-portrait-core-services-sw-v-1-2-0-ref-5700592-patient-monitoring-system/) A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed patient alarms, and/or access to Protected Health Information (PHI). Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the state of MI, and the countries of Czech Republic, Finland, Germany, Netherland, Qatar, UAE. [Official source for GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2878-2026%22) Jun 29, 2026 FDA device enforcement ### [GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph](https://isitonrecall.com/recall/fda-device-z-2876-2026-ge-healthcare-mac-vu360-ref-part-number-2030361-023-electrocardiograph/) Software issue issue with the MAC VU360 v3.0 system. After selecting the order refresh icon, an open preview or review screen might fail to close automatically after 2 minutes of inactivity. As a result, data from a previous patient may remain on the screen... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Belgium, Hong Kong, Netherlands, Sweden, UK. [Official source for GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2876-2026%22) Apr 24, 2026 FDA device enforcement ### [GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physi...](https://isitonrecall.com/recall/fda-device-z-2242-2026-ge-healthcare-carescape-telemetry-server-v5-ato-model-ref-2063702-101-product-code-ss9-used-in-conju/) GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central ... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used i...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2242-2026%22) Apr 24, 2026 FDA device enforcement ### [GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service only, REF #2108523-01; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor...](https://isitonrecall.com/recall/fda-device-z-2243-2026-ge-healthcare-apexpro-v5-0-ark2250-software-disaster-recovery-usb-kit-orderable-by-ge-service-only-r/) GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central ... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Servi...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2243-2026%22) Apr 24, 2026 FDA device enforcement ### [GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(Wit...](https://isitonrecall.com/recall/fda-device-z-2244-2026-ge-healthcare-iou-assy-ark2250-carescape-telemetry-server-ref-2108729-901-product-code-ss9-apexpro-c/) GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central ... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; Ap...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2244-2026%22) Apr 24, 2026 FDA device enforcement ### [GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monit...](https://isitonrecall.com/recall/fda-device-z-2245-2026-ge-healthcare-carescape-telemetry-server-ark-2250l-north-america-ref-5697603-product-code-ksa-used-i/) GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central ... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KS...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2245-2026%22) Apr 24, 2026 FDA device enforcement ### [GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS...](https://isitonrecall.com/recall/fda-device-z-2246-2026-ge-healthcare-trade-in-carescape-telemetry-server-ark-2250l-north-america-ref-5697603-902-product-co/) GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central ... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Pr...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2246-2026%22) Apr 24, 2026 FDA device enforcement ### [GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Pa...](https://isitonrecall.com/recall/fda-device-z-2247-2026-ge-healthcare-apexpro-v6-0-edelivery-software-ref-5700026-product-code-suv-used-in-conjunction-wtih/) GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central ... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunctio...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2247-2026%22) Apr 24, 2026 FDA device enforcement ### [CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3](https://isitonrecall.com/recall/fda-device-z-2279-2026-case-v7-0-cardiac-testing-system-model-no-3031234-001-product-code-su3/) Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer head can result in charring or discoloration of thermal printer paper. Ignition of the paper could po... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Algeria, Australia, Bangladesh, Cambodia, Canada, Croatia, Denmark, Finland, France, Germany, Greece, Hong Kong, Indi... [Official source for CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2279-2026%22) Apr 25, 2025 FDA device enforcement ### [MUSE 5 Systems, Model Numbers 2021274-001, 2023032-005, 2027478-001, Large capacity client-server-based computer system that accesses stores and manages cardiovascular information.](https://isitonrecall.com/recall/fda-device-z-1938-2025-muse-5-systems-model-numbers-2021274-001-2023032-005-2027478-001-large-capacity-client-server-based/) The MUSE Administrator Account active directory or local credential could potentially be used from your local network to log into a GE HealthCare MUSE 5 system and potentially manipulate recorded patient data. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for MUSE 5 Systems, Model Numbers 2021274-001, 2023032-005, 2027478-001, Large capacity client-server...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1938-2025%22) Apr 22, 2024 FDA device enforcement ### [Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX electrophysiology recording system and ComboLab AltiX hemodynamic and electrophysiology recording system; and Field R...](https://isitonrecall.com/recall/fda-device-z-2258-2024-prucka-3-amplifier-model-p1801pa-used-with-cardiolab-altix-electrophysiology-recording-system-and-co/) Capacitors in certain Prucka 3 Amplifiers used with CardioLab / ComboLab systems could fail resulting in transient oscillations on the display and inability to view surface and intracardiac ECG waveforms. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AK, AZ, CA, CO, FL, GA, IL, KY, MA, ME, MN, MO, NC, NJ, NY, OH, OR, PA, TN, TX, and WA. The countries of Belgium, Canada,... [Official source for Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX electrophysiology recording system an...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2258-2024%22) Apr 9, 2024 FDA device enforcement ### [GE HealthCare CRITIKON ONE-CUF blood pressure cuffs, Model numbers: 1. ONE-A1-1B, ONE-CUF, SMALL ADULT, 1 TB BAYONET, 17 - 25 CM, 20/BOX; 2. ONE-A1-2A, ONE-CUF, SMALL ADULT, DIN...](https://isitonrecall.com/recall/fda-device-z-2027-2024-ge-healthcare-critikon-one-cuf-blood-pressure-cuffs-model-numbers-1-one-a1-1b-one-cuf-small-adult-1/) Use of the blood pressure cuffs could result in inaccurate non-invasive blood pressure measurements. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, AR, AZ, CA, FL, GA, IA, IL, IN, LA, MD, MO, MS, NC, NJ, NM, OH, PA, TN, and TX. [Official source for GE HealthCare CRITIKON ONE-CUF blood pressure cuffs, Model numbers: 1. ONE-A1-1B, ONE-CUF, SMALL ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2027-2024%22) Aug 8, 2023 FDA device enforcement ### [Prucka 3 Amplifiers, Model P1801PA, and Field Replaceable Units (FRUs), Model 5875569, used with CardioLab AltiX and ComboLab AltiX.](https://isitonrecall.com/recall/fda-device-z-2613-2023-prucka-3-amplifiers-model-p1801pa-and-field-replaceable-units-frus-model-5875569-used-with-cardiolab/) A diode on the power supply of the Prucka 3 Amplifier used with CardioLab/ComboLab systems could reach elevated temperatures and fail, then power off and become inoperable. Class II Reported ongoing Distribution: Distribution was made to CA, CO, FL, GA, IL, IN, KY, MA, NC, NJ, OH, OR, PA, SC, TX, VA, and WI. There was government distribution but no military distribution. Foreign distribu... [Official source for Prucka 3 Amplifiers, Model P1801PA, and Field Replaceable Units (FRUs), Model 5875569, used with ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2613-2023%22) ## Reasons in these listed records - Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events. - Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or care area. - A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed patient alarms, and/or access to Protected Health Information (PHI). - Software issue issue with the MAC VU360 v3.0 system. After selecting the order refresh icon, an open preview or review screen might fail to close automatically after 2 minutes of inactivity. As a result, data from a previous patient may remain on the screen and could be incorr... These examples come from this result page and are not a ranking of every recall reason. ## Checking GE Medical Systems Information Technologies Inc ### Is there a recall on ge medical systems information technologies inc right now? This archive contains 18 records, including 18 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 Information Technologies Inc](https://isitonrecall.com/check/?q=GE%20Medical%20Systems%20Information%20Technologies%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)