GE Medical Systems, LLC
93 recalls on record · Latest: Dec 17, 2025
GE Medical Systems, LLC Recall Insight
GE Medical Systems, LLC appears on 93 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.111% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Dec 17, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.
On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 48 of 50 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Aug 14, 2024 to Dec 17, 2025.
Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.
Senographe Pristina, Pristina Serena, and Pristina Serena 3D. for screening and diagnostic mammography
MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model Number 2030360-001, Product Cod…
LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535
LOGIQ P9 R4.5 ultrasound system with system software version R4.5.7., Model Number 5877533
GE HealthCare OEC 9900 Elite C-arm Systems.
GE HealthCare OEC 9800.
GE Signa Artist, Nuclear Magnetic Resonance Imaging System
GE SIGNA Premier Elite (China Only), Nuclear Magnetic Resonance Imaging System
GE SIGNA Premier XT (China Only), Nuclear Magnetic Resonance Imaging System
GE Signa Voyager, Nuclear Magnetic Resonance Imaging System
GE Discovery MR750 3.0T, Nuclear Magnetic Resonance Imaging System
GE Discovery MR450 1.5T, Nuclear Magnetic Resonance Imaging System
GE SIGNA Hero XT (China Only), Nuclear Magnetic Resonance Imaging System
GE SIGNA Artist Evo, Nuclear Magnetic Resonance Imaging System
GE SIGNA PET/MR AIR (China Only), Nuclear Magnetic Resonance Imaging System
GE SIGNA PET/MR, Tomographic Imager Combining Emission Computed Tomography with Nuclear Magnetic Resonance
GE SIGNA Hero Elite (China Only), Nuclear Magnetic Resonance Imaging System
GE SIGNA Voyager AIR (China Only), Nuclear Magnetic Resonance Imaging System
GE SIGNA PET/MR AIR Plus (China Only), Nuclear Magnetic Resonance Imaging System
GE SIGNA Hero MAX (China Only), Nuclear Magnetic Resonance Imaging System
GE SIGNA Architect AIR (China Only), Nuclear Magnetic Resonance Imaging System
SIGNA Architect
SIGNA Architect AIR
OEC Elite: The OEC Elite mobile C-arm is intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/device…
Venue Go Models: R2 (Model Number H45181VG), R3 (Model Number H45193VG), R4 (Model Number H45114VG), R5 (Model Numbers H45135VG, H45135VGW), R3 Surge…
GE Healthcare Revolution Apex, System, X-ray, Tomography, Computed
GE Healthcare Revolution Apex Select, System, X-ray, Tomography, Computed
GE Healthcare Revolution CT, System, X-ray, Tomography, Computed
Optima XR646 HD. X-Ray imaging system.
Definium 656HD & Discovery XR656HD (GTINs: 00840682138598, 00195278840226, 00840682136709). X-Ray imaging system.
Discovery XR656 HD. X-Ray imaging system.
Portrait Core Services, a set of software services that enable the communication and interaction of the Portrait Mobile Monitoring Solution component…
Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO
Tec 850 SEV Anesthesia Vaporizer, Reference Number 1177-9850-SEV
GE Healthcare Optima XR220amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-12; 2) 5555000-5; 3) 5555000-6; 4) A0659PB; 5…
GE Healthcare Optima XR200amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-3; 2) 5555000-4: 3) A0659MB
GE Healthcare Optima XR240amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-27; 2) 5555000-31; 3) 5555000-33; 4) 5555000-4…
SIGNA Architect AIR, Nuclear Magnetic Resonance Imaging System
Discovery MR750w 3.0T, whole body magnetic resonance scanner
SIGNA Architect, Nuclear Magnetic Resonance Imaging System
SIGNA Explorer, with affected software versions: SV25.5, SV25.6, SV29.2, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
SIGNA Architect, with affected software versions: DV26.0 to DV26.3, DV27.0 to DV27.3, DV28.0 to DV28.5, DV29.0, DV29.1, DV29.2, MR30.0, MR30.1; Nucl…
SIGNA MR355, with affected software versions: SV25.5, SV25.6; Nuclear Magnetic Resonance Imaging System
SIGNA PET/MR, with affected software versions: MP24.0, MP26.0, MP26.1, MR30.0, MR30.1; Tomographic imager combining emission computed tomography wit…
Discovery MR450 1.5T, with affected software versions: DV24.0, DV25.0, DV25.1, DV26.0; Nuclear Magnetic Resonance Imaging System
SIGNA Voyager, with affected software versions: PX26.0 to PX26.6, VX28.0, VX29.1, VX29.2, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
Optima MR360, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
SIGNA UHP, with affected software versions: RX28.0, MR30.1; Nuclear Magnetic Resonance Imaging System - research use only
SIGNA MR380, with affected software versions: SV25.5, SV25.6; Nuclear Magnetic Resonance Imaging System
SIGNA MR360, with affected software versions: SV25.5, SV25.6; Nuclear Magnetic Resonance Imaging System
Nearby Manufacturers
Other firms with recall activity tracked in the PlainRecalls index.
Data Sources
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