Every recall we track for GE Medical Systems Information Technologies Inc — 19 in all — plus the complaints and injury reports the public filed about them.
GE Medical Systems recalls Portrait Core Services Software V1.1 (Ref# 5700209) due to potential loss of patient monitoring and alarm reset issues. Affected units may require correction to prevent safety risks.
GE Medical Systems recalls Portrait Core Services SW Reload V1.1 software update that may cause loss of patient monitoring and reset alarm settings to factory defaults.
GE Medical Systems recalls Portrait Compute V1.2 software update (Ref# 5700592) due to potential loss of patient monitoring and alarm reset issues. Affected units may require correction to prevent safety risks.
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 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 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 HealthCare recalls specific CARESCAPE Telemetry Server V5 models due to potential loss of ECG and SpO2 monitoring if the system enters a persistent NO COMM or OFF NETWORK state.
GE HealthCare recalls APEXPRO v5.0 software for potential ECG and SpO2 monitoring loss if network disconnects occur. Affected units may require service.
GE HealthCare recalls specific telemetry servers due to potential loss of ECG and SpO2 monitoring if network disconnects occur. Affected units may need repair or update to prevent patient monitoring issues.
GE Healthcare offers a wide range of medical imaging systems including CT, MRI, X-ray, and ultrasound equipment for clinical and research applications.
GE HealthCare recalls CARESCAPE Telemetry Server ARK-2250L (North America, Ref #5697603) used with ApexPro CTS v6.0. Potential loss of ECG and SpO2 monitoring due to persistent NO COMM or OFF NETWORK conditions. Affected units have specific serial numbers listed.
GE HealthCare recalls ApexPro v6.0 eDelivery Software (REF #5700026) used with ApexPro CARESCAPE Telemetry Server. Potential loss of ECG and SpO2 monitoring due to persistent NO COMM or OFF NETWORK conditions. No remedy specified.
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 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 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 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 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.
