GE Medical Systems, LLC recalls
Every recall we track for GE Medical Systems, LLC — 130 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from GE Medical Systems, LLC peaked in 2025 (48); 130 since 2017. 1% rated “stop using now”.
All FDA recall records for GE Medical Systems, LLC 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 | 0 | 0 | 0 |
| 2018 | 0 | 3 | 3 | 0 | 6 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 8 | 7 | 0 | 15 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 28 | 10 | 1 | 39 |
| 2025 | 1 | 30 | 17 | 0 | 48 |
| 2026 (to date) | 0 | 9 | 9 | 4 | 22 |
What to do if you have a recalled GE Medical Systems, LLC 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, LLC recalls
28 shown- Use cautionMedical device
GE Medical Systems, LLC recalls Optima XR200amx, Mobile Digital-Ready Radiographic System
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 Medical SystemsJun 5, 2026 - Use cautionMedical device
GE Medical Systems, LLC recalls Giraffe OmniBed Field Replaceable Unit (FRU), Model Numbers 6600-1056-400 and 6600-1461-500
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 SystemsMay 1, 2026 - Use cautionMedical device
GE Medical Systems, LLC recalls Allia IGS 3 Pulse angiographic X-ray system
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 SystemsApr 20, 2026 - UnratedMedical device
GE Medical Systems, LLC recalls Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15
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 SystemsMar 26, 2026 - Lower riskMedical device
GE Medical Systems, LLC recalls Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and
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 Medical SystemsFeb 3, 2026 - Lower riskMedical device
GE Medical Systems, LLC recalls Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images
GE Medical Systems, LLC
GE Medical Systems, LLCJan 30, 2026 - Lower riskMedical device
GE Medical Systems, LLC recalls Senographe Pristina, Pristina Serena, and Pristina Serena 3D. for screening and diagnostic mammography
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 SystemsOct 24, 2025 - Lower riskMedical device
GE Medical Systems, LLC recalls LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535
GE Medical recalls LOGIQ P10 R4.5 HD ultrasound systems with software version R4.5.7. Model 5877535 may show inaccurate liver fat measurements, risking wrong medical decisions.
GE MedicalSep 18, 2025 - Lower riskMedical device
GE Medical Systems, LLC recalls MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model
GE Healthcare is a global leader in medical technology, providing innovative solutions for healthcare professionals worldwide.
GE Medical SystemsAug 22, 2025 - Lower riskMedical device
GE Medical Systems, LLC recalls GE HealthCare OEC 9900 Elite C-arm Systems.
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 HealthCareJul 2, 2025 - Use cautionMedical device
GE Medical Systems, LLC recalls GE Signa Artist, Nuclear Magnetic Resonance Imaging System
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 HealthcareJun 20, 2025 - Lower riskMedical device
GE Medical Systems, LLC recalls SIGNA Architect
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 SystemsMay 23, 2025 - Lower riskMedical device
GE Medical Systems, LLC recalls OEC Elite: The OEC Elite mobile C-arm is intended to provide fluoroscopic and digital spot images of the patient
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 SystemsMar 21, 2025 - Stop using nowMedical device
GE Medical Systems, LLC recalls Venue Go Models: R2 (Model Number H45181VG), R3 (Model Number H45193VG), R4 (Model Number H45114VG), R5 (Model 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 Medical SystemsMar 6, 2025 - Use cautionMedical device
GE Medical Systems, LLC recalls GE Healthcare Revolution Apex, System, X-ray, Tomography, Computed
GE Healthcare recalls certain Revolution Apex and Revolution CT systems due to potential blue coolant leak near gantry base that could cause slips and falls. No immediate action needed but check for leaks.
GE HealthcareFeb 18, 2025 - Lower riskMedical device
GE Medical Systems, LLC recalls Optima XR646 HD. X-Ray imaging system.
GE Medical Systems recalls Optima XR646 HD X-Ray systems that may allow continued imaging after reaching exposure limits without user acknowledgment, potentially causing overexposure. Affected units have GTIN 0019527:526892.
GE Medical SystemsJan 28, 2025 - Lower riskMedical device
GE Medical Systems, LLC recalls Portrait Core Services, a set of software services that enable the communication and interaction of the Portrait Mobile
GE Medical Systems recalls Portrait Core Services software that may lose patient monitoring after 425 days of continuous use. Affected units include specific model CSSXB with serial numbers listed. No remedy provided in recall notice.
GE Medical SystemsDec 6, 2024 - Use cautionMedical device
GE Medical Systems, LLC recalls GE Healthcare Optima XR220amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-12; 2) 5555000-5; 3)
GE Healthcare recalls Optima XR220amx mobile radiography systems with missing safety bolts that could cause arm drop if internal cable fails.
GE HealthcareNov 25, 2024 - Use cautionMedical device
GE Medical Systems, LLC recalls Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO
GE Medical Systems recalls Tec 820 ISO Anesthesia Vaporizers with specific serial numbers due to potential delivery of less anesthetic than set by the dial, which could lead to inadequate anesthesia during surgery.
GE Medical SystemsNov 18, 2024 - Use cautionMedical device
GE Medical Systems, LLC recalls SIGNA Architect AIR, Nuclear Magnetic Resonance Imaging System
GE Medical Systems recalls SIGNA Architect AIR MRI systems with specific UDI codes due to potential elevated acoustic noise during scans. Affected units may require correction to prevent hearing damage.
GE HealthcareOct 28, 2024 - Use cautionMedical device
GE Medical Systems, LLC recalls SIGNA Explorer, with affected software versions: SV25.5, SV25.6, SV29.2, MR30.0, MR30.1; Nuclear Magnetic Resonance
GE Medical Systems recalls SIGNA Explorer MRI systems with software versions SV25.5, SV25.6, SV29.2, MR30.0, MR30.1. These versions may cause overheating of MR conditional implants when scanning in Low SAR Mode with specific imaging sequences.
GEJun 14, 2024 - Lower riskMedical device
GE Medical Systems, LLC recalls B105P Patient Monitor (with E-module slot option), REF 6160000-001-XXXXXX,
GE Medical Systems recalls certain B105P Patient Monitors with E-module slot that may display inaccurate CO2 readings when used in locations not at or near sea level. This could affect medical monitoring accuracy.
GE Medical SystemsNov 16, 2022 - Use cautionMedical device
GE Medical Systems, LLC recalls Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ
GE Medical Systems recalls Vivid S6 ultrasound systems used in fetal/obstetrics, abdominal/GYN, pediatric, and small organ imaging. Batteries not replaced at 2 years (as per Service Manual) may fail or emit smoke/catch fire. Affected models listed in the recall.
GE Medical SystemsNov 10, 2022 - Lower riskMedical device
GE Medical Systems, LLC recalls Centricity Universal Viewer 6.0. Used to display medical images (Including mammograms) and data from various imaging
GE Medical Systems recalls Centricity Universal Viewer 6.0 software that may hide medical studies without user notification, potentially delaying diagnosis. Affected units have specific product IDs listed in the recall.
GE Medical SystemsOct 28, 2022 - Use cautionMedical device
GE Medical Systems, LLC recalls SIGNA Architect system Product Usage: The Signa Architect system is a whole body magnetic resonance scanner designed to
GE Medical Systems recalls Signa Architect MRI systems with specific serial numbers due to potential serious burns if patient touches warm bore surface without proper padding. Affected units may need safety adjustments.
GE Medical SystemsOct 3, 2018 - Lower riskMedical device
GE Medical Systems, LLC recalls GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T
GE Healthcare recalls MRI systems with software version 11.x due to potential image flips left/right and patient data mismatches after service activities. Affected models include 1.5T and 3.0T systems with specific serial numbers.
GE HealthcareJun 7, 2018 - Use cautionMedical device
GE Medical Systems, LLC recalls Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the following product name sold under: Product
GE Medical Systems recalls Discovery MR750w MRI systems with a warm bore surface that can cause serious burns if patient touches it without proper padding. Affected models include 3.0T MR750W variants with specific serial numbers. Contact GE for details.
GE Medical SystemsJun 6, 2018 - Use cautionMedical device
GE Medical Systems, LLC recalls MR Surgical Suite Option Product The MR Surgical Option when integrated with the GE Signa¿ 3.0T or 1.5T magnetic
GE Medical Systems recalls MR Surgical Option products with GE Signa 3.0T or 1.5T scanners due to potential patient transfer mechanism failure during surgery. Affected models include M8074SS, M8053SS, and others. Contact GE for remedy.
GE Medical SystemsMar 30, 2018
GE Medical Systems, LLC recall questions
How many recalls has GE Medical Systems, LLC had?
130 recalls from GE Medical Systems, LLC are on record with U.S. safety agencies, from 2018–2026.
What is the most recent GE Medical Systems, LLC recall?
GE Medical Systems, LLC recalls Optima XR200amx, Mobile Digital-Ready Radiographic System, dated Jun 5, 2026. Every GE Medical Systems, LLC recall is listed on this page, newest first.
What should I do if I have a recalled GE Medical Systems, LLC 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, LLC 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.