Every recall we track for GE Medical Systems, LLC — 130 in all — plus the complaints and injury reports the public filed about them.
GE Medical Systems recalls Optima XR240amx mobile X-ray systems with potential column safety failure causing patient injury during exams. Affected units have specific system IDs and UDI-DI numbers.
GE Healthcare recalls Optima XR220amx mobile X-ray systems with potential safety pawl failure causing arm drop during exams. Affected units have specific system IDs; contact GE for details.
GE Medical Systems recalls Optima XR20:00amx mobile radiography systems with potential column safety failure causing patient injury during exams. Affected units have specific system IDs and were sold from February 2010.
GE Healthcare is a global leader in medical technology, providing innovative solutions for healthcare professionals worldwide.
GE Healthcare provides innovative medical imaging, diagnostics, and life sciences solutions for healthcare professionals worldwide.
GE Medical Systems recalls Giraffe OmniBed Field Replaceable Units with specific model numbers due to potential disengagement of fasteners that could fall into patient compartment, risking injury.
GE Medical Systems recalls Allia IGS 7 Pulse angiographic X-ray systems with specific serial numbers due to potential electrical shock risk during installation or maintenance when power is on. Affected units require immediate attention from service personnel.
GE Medical Systems recalls Allia IGS 5 Pulse angiographic X-ray systems with specific serial numbers due to potential electrical shock hazard for service personnel during installation or maintenance when power is on.
GE Medical Systems recalls Allia Moveo angiographic X-ray systems with specific serial numbers due to potential electrical shock risk for service personnel during installation or maintenance when power is on.
GE Medical Systems recalls Allia IGS Pulse angiographic X-ray systems with potential electrical shock risk for service personnel during installation or maintenance. Affected units have specific serial numbers and UDI-DI codes.
GE Medical Systems recalls Allia IGS 3 Pulse angiographic X-ray systems with potential electrical shock risk during installation or maintenance. Affected units have specific serial numbers and UDI-DI codes.
GE Medical Systems recalls Revolution CT scanners with model numbers 5590000 and 5590000-6 due to potential security vulnerabilities in their EHL-based CT Smart Subscription software.
GE Medical Systems recalls Revolution Apex Plus CT scanners with specific model numbers due to a potential security vulnerability in the AW Server used with Edison Health Link. This could allow unauthorized access to patient data.
GE Medical Systems recalls Revolution Apex CT scanners with specific model numbers due to a potential security vulnerability in the AW Server used with Edison Health Link. This could impact patient data security.
GE Healthcare recalls Revolution Apex Elite CT scanners with specific model numbers due to a potential security vulnerability in their AW Server software that could impact patient data safety.
GE Medical Systems recalls Revolution Apex Select CT scanners with model 5590000-27 due to potential security vulnerabilities in EHL-based CT Smart Subscription systems.
GE Medical Systems recalls Revolution Ascend CT scanners with specific model numbers due to a potential security vulnerability in the AW Server used with Edison Health Link. Affected units may be at risk of security breaches.
GE Medical Systems recalls Revolution CT ES X-ray CT scanners with model 5590000-15 due to a security vulnerability in the AW Server that could expose patient data. Affected units include specific serial numbers listed in the recall notice.
GE Medical Systems recalls Imactis CT-Navigation System stereotaxic accessories (models E85101LA/E85101LP) due to potential mismatch between simulated and actual needle trajectories during CT procedures.
GE Healthcare provides a wide range of medical imaging solutions including MRI, CT, X-ray, and more.
GE Medical Systems recalls Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1 due to potential cybersecurity vulnerability that could expose user login credentials on local workstations.
GE Medical Systems, LLC
GE Medical Systems recalls Senographe Pristina, Pristina Serena, and Pristina Serena 3D mammography machines due to a missing or incorrect X-Ray Warning label, a nonconformance with FDA regulations.
GE Medical recalls LOGIQ P10 ultrasound devices with software version R4.5.7 that may show inaccurate liver fat measurements, potentially leading to incorrect medical decisions.
GE Medical recalls LOGIQ P9 R4.5 ultrasound systems with software version R4.5.7 (model 5877533) due to potential inaccurate liver steatosis measurements, which could lead to inappropriate clinical decisions.
GE Medical Systems recalls LOGIQ P10 R4.5 HD ultrasound systems with software version R4.5.7. Model 5877535 may display inaccurate liver fat measurements, risking wrong medical decisions.
GE Healthcare is a global leader in medical technology, providing innovative solutions for healthcare professionals worldwide.
GE HealthCare recalls OEC 9800 C-arm systems with missing lead tape, increasing radiation exposure. Affected units may not be detectable by users. Contact GE for details.
GE HealthCare recalls OEC 9900 Elite C-arm systems with missing lead tape, increasing radiation exposure risk. Affected units may require repair or replacement.
GE Medical Systems recalls SIGNA Hero MRI systems with unverified caster lock maintenance since March 2023. This could lead to patient table instability during scans. Affected units need verification via system ID numbers.
GE recalls certain Optima MR450w 1.5T MRI systems due to potential failure in patient table caster locks during maintenance. This could affect patient safety if the table moves unexpectedly.
GE recalls SIGNA Premier MRI systems where table caster locks may not have been checked during maintenance since March 2023. This could lead to patient table movement during scans.
GE Healthcare recalls certain MRI systems due to potential failure of patient table caster locks during maintenance. Affected units include Discovery MR750w 3.0T models with specific system IDs from March 2023 onward.
GE recalls SIGNA Architect MRI systems where table caster locks may not have been checked during maintenance since March 2023. Owners should contact GE for repair if they had maintenance after that date.
GE Medical Systems recalls China-only SIGNA Premier MAX MRI systems where table locks may not have been checked during maintenance since March 2023. Affected units require verification of maintenance history.
GE Medical Systems recalls certain SIGNA Architect AIR MRI systems sold in China due to potential failure in caster lock maintenance checks. Affected units were serviced after March 1, 2023. No immediate action is required but ensure maintenance checks are completed.
GE Medical Systems recalls SIGNA Hero MAX MRI systems sold in China due to potential caster lock failure during maintenance. Affected units have system IDs from March 2023. No immediate action required but check for maintenance records.
GE Medical Systems recalls certain SIGNA PET/MR AIR Plus MRI systems sold in China due to potential failure in caster lock maintenance steps, which could affect patient safety during imaging procedures.
GE Medical Systems recalls certain SIGNA Voyager AIR MRI systems sold in China due to potential failure of patient table caster locks during maintenance. Affected units have system IDs from March 2023 onwards. No immediate action required but check for maintenance records.
GE Medical Systems recalls certain SIGNA Hero Elite MRI systems sold in China due to potential failure of patient table caster locks during maintenance. Affected units were serviced after March 1, 2023. No immediate action required but check system ID numbers.
GE Medical Systems recalls certain SIGNA PET/MR MRI scanners that may not have had caster locks checked during maintenance, potentially causing patient table movement during use.
GE Medical Systems recalls certain SIGNA PET/MR AIR MRI systems sold in China due to potential failure in patient table caster locks during maintenance. Affected units have system IDs from March 2023 maintenance. No immediate action needed but check for recall details.
GE Medical Systems recalls SIGNA Artist Evo MRI systems where caster locks weren't properly checked during maintenance since March 2023, potentially causing patient table instability.
GE Medical Systems recalls certain SIGNA Hero XT MRI systems sold in China due to unperformed caster lock maintenance. This could affect patient safety during imaging procedures. Affected units have system IDs from March 2023 maintenance.
GE Medical Systems recalls certain Discovery MR450 1.5T MRI systems due to potential failure in caster lock maintenance, which could lead to patient table instability during use.
GE Healthcare recalls certain Discovery MR750 3.0T MRI systems due to potential caster lock failure if maintenance steps weren't completed. Affected units were serviced since March 2023.
GE recalls Signa Voyager MRI systems where table caster locks may not have been checked during maintenance since March 2023. Owners should contact GE for a free inspection.
GE Medical Systems recalls China-only SIGNA Premier XT MRI systems due to potential table lock failure during maintenance. Affected units have system IDs from March 2023 maintenance. No immediate action needed but check for maintenance records.
GE Medical Systems recalls certain SIGNA Premier Elite MRI systems sold in China due to potential failure in caster lock maintenance checks, which could affect patient safety during imaging procedures.
GE Healthcare recalls certain Signa MRI systems due to potential failure of patient table caster locks during maintenance. Affected units were serviced since March 2023; owners should contact GE for details.
GE Medical Systems recalls Discovery MR750w 3.0T MRI systems due to potential acoustic noise exceeding 99dB during scans, which may exceed hearing protection limits.
GE Medical Systems recalls SIGNA PET/MR systems with gradient coils that may produce excessive noise (over 99dB) during scans, exceeding safe hearing protection limits.
GE Medical Systems recalls SIGNA Architect AIR MRI gradient coils that may produce excessive noise (over 99dB) during scans, exceeding safe hearing levels without proper protection.
GE Medical Systems recalls SIGNA Architect MRI gradient coils that can produce loud noise over 99dB during scans, potentially exceeding hearing protection limits. Affected units have specific GTINs listed in the recall notice.
GE Medical Systems recalls OEC Elite and OEC 3D Mobile C-arm systems that may exceed 4% source-to-image distance in X-ray field, potentially causing radiation exposure. Systems with serial numbers listed in Appendix A are affected.
GE Medical Systems recalls OEC Elite and OEC 3D Mobile C-Arms that may exceed 4% source-to-image distance in X-ray field, potentially affecting safety during medical procedures. Systems with specific serial numbers listed in Appendix A are affected.
GE Medical Systems recalls Venue Fit R3, R4, and R5 ultrasound systems with specific model numbers due to potential battery failure causing smoke or fire. Affected units include China versions and certain serial numbers.
GE Medical Systems recalls Venue Go ultrasound systems R2-R5 models with potential battery failure causing smoke or fire. Affected units include specific model numbers and China versions. Stop using immediately to avoid fire risk.
GE Healthcare is recalling certain Revolution Apex Elite and Revolution CT systems due to potential blue coolant fluid leaks near the gantry base. The fluid is not corrosive or hot but can cause slips and falls if unnoticed. No remedy is specified in the recall notice.
