GE Medical Systems Information Technologies Inc recalls
Every recall we track for GE Medical Systems Information Technologies Inc — 20 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
20 recalls since 2017.
All FDA recall records for GE Medical Systems Information Technologies Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 1 | 0 | 0 | 1 |
| 2024 | 0 | 0 | 2 | 0 | 2 |
| 2025 | 0 | 0 | 1 | 0 | 1 |
| 2026 (to date) | 0 | 6 | 7 | 1 | 14 |
What to do if you have a recalled GE Medical Systems Information Technologies Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All GE Medical Systems Information Technologies Inc recalls
12 shown- Lower riskMedical device
GE Medical Systems Information Technologies Inc recalls Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04, 5867474-13 Product code STU CSCS V3 MAI800
GE Medical Systems recalls Carescape Central Station V3 MAS800 desktop units with part numbers 5867474-04 and 5867474-13. The device may delay patient monitoring for up to 3 minutes after restart, risking missed critical health events.
GE Medical SystemsJul 30, 2026 - Use cautionMedical device
GE Medical Systems Information Technologies Inc recalls PORTRAIT CORE SERVICES SOFTWARE V1.0.5, Ref# 5697353
GE Medical Systems recalls Portrait Core Services Software V1.0.5 (Ref# 5697353) due to potential loss of patient monitoring and alarm reset issues. Affected units may require software updates to prevent safety risks.
GE Medical SystemsJul 20, 2026 - Use cautionMedical device
GE Medical Systems Information Technologies Inc recalls GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system
GE Healthcare recalls patient monitoring software version 1.2.0 (REF 5700592) due to a software vulnerability that could allow unauthorized access to patient data and monitoring systems.
GE HealthcareJul 10, 2026 - Lower riskMedical device
GE Medical Systems Information Technologies Inc recalls GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph
GE Healthcare recalls MAC VU360 electrocardiograph models with serial numbers listed. Software issue may cause previous patient data to remain on screen and be incorrectly linked to new patients during use.
GE HealthcareJun 29, 2026 - Lower riskMedical device
GE Medical Systems Information Technologies Inc recalls CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
GE Healthcare offers a wide range of medical imaging systems including CT, MRI, X-ray, and ultrasound equipment for clinical and research applications.
GEApr 24, 2026 - Lower riskMedical device
GE Medical Systems Information Technologies Inc recalls GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used
GE HealthCare recalls specific CARESCAPE Telemetry Server ARK-2250L models (North America) due to potential loss of ECG and SpO2 monitoring in certain network conditions. Affected units have serial numbers starting with KSA.
GE HealthCareApr 24, 2026 - Lower riskMedical device
GE Medical Systems Information Technologies Inc recalls MUSE 5 Systems, Model Numbers 2021274-001, 2023032-005, 2027478-001, Large capacity client-server-based computer system
GE Medical Systems recalls MUSE 5 Systems with model numbers 2021274-001, 2023032-005, 2027478-001. These systems could allow unauthorized access to patient data via active directory credentials. Affected units include specific serial numbers listed in the recall notice.
GE Medical SystemsApr 25, 2025 - Lower riskMedical device
GE Medical Systems Information Technologies Inc recalls Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX electrophysiology recording system and ComboLab AltiX
GE Medical recalls Prucka 3 Amplifier Model P1801PA used with CardioLab/ComboLab systems due to capacitor failure causing display oscillations and ECG waveform issues. Affected units have specific serial numbers.
GE Medical SystemsApr 22, 2024 - Lower riskMedical device
GE Medical Systems Information Technologies Inc recalls GE HealthCare CRITIKON ONE-CUF blood pressure cuffs, Model numbers: 1. ONE-A1-1B, ONE-CUF, SMALL ADULT, 1 TB BAYONET,
GE HealthCare recalls ONE-CUF blood pressure cuffs (models 1-12) due to potential inaccurate blood pressure readings. Affected units include adult, child, and infant sizes with specific model numbers and GTINs. No remedy is provided in the recall notice.
GE HealthCareApr 9, 2024 - Use cautionMedical device
GE Medical Systems Information Technologies Inc recalls Prucka 3 Amplifiers, Model P1801PA, and Field Replaceable Units (FRUs), Model 5875569, used with CardioLab AltiX and
GE Medical Systems recalls Prucka 3 Amplifiers (Model P1801PA) and Field Replaceable Units (Model 5875569) used with CardioLab AltiX systems due to potential power supply failure causing inoperability.
GE Medical SystemsAug 8, 2023 - Lower riskMedical device
GE Medical Systems Information Technologies, Inc. recalls GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The CARESCAPE Central Station is intended to
GE Healthcare recalls CARESCAPE Central Station software version 2.0.2 units that may experience unexpected NO COMM (No Communication) and network communication issues after boot-up or system restart. Affected units have specific model numbers and serial numbers listed in the recall.
GE HealthcareJan 11, 2018 - Lower riskMedical device
GE Medical Systems Information Technologies, Inc. recalls CARESCAPE Patient Data Module (PDM) v2.6 software used with CARESCAPE Monitors B850, B650, and B450 v2.0.7 or earlier
GE Medical Systems recalls CARESCAPE Patient Data Module v2.6 software used with CARESCAPE Monitors B850, B650, and B450 v2.0.7 or earlier. This software fails to produce visual or audible alarms for impedance respiration apnea events, potentially missing critical patient safety alerts.
GE Medical SystemsJul 13, 2017
GE Medical Systems Information Technologies Inc recall questions
How many recalls has GE Medical Systems Information Technologies Inc had?
20 recalls from GE Medical Systems Information Technologies Inc are on record with U.S. safety agencies, from 2017–2026.
What is the most recent GE Medical Systems Information Technologies Inc recall?
GE Medical Systems Information Technologies Inc recalls Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04, 5867474-13 Product code STU CSCS V3 MAI800, dated Jul 30, 2026. Every GE Medical Systems Information Technologies Inc recall is listed on this page, newest first.
What should I do if I have a recalled GE Medical Systems Information Technologies Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new GE Medical Systems Information Technologies Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.