PlainRecalls

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.

FDA Devices Moderate Dec 17, 2025

Senographe Pristina, Pristina Serena, and Pristina Serena 3D. for screening and diagnostic mammography

FDA Devices Moderate Oct 29, 2025

MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model Number 2030360-001, Product Cod…

FDA Devices Moderate Oct 22, 2025

LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535

FDA Devices Moderate Oct 22, 2025

LOGIQ P9 R4.5 ultrasound system with system software version R4.5.7., Model Number 5877533

FDA Devices Moderate Sep 3, 2025

GE HealthCare OEC 9900 Elite C-arm Systems.

FDA Devices Moderate Sep 3, 2025

GE HealthCare OEC 9800.

FDA Devices Moderate Aug 20, 2025

GE Signa Artist, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA Premier Elite (China Only), Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA Premier XT (China Only), Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE Signa Voyager, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE Discovery MR750 3.0T, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE Discovery MR450 1.5T, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA Hero XT (China Only), Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA Artist Evo, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA PET/MR AIR (China Only), Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA PET/MR, Tomographic Imager Combining Emission Computed Tomography with Nuclear Magnetic Resonance

FDA Devices Moderate Aug 20, 2025

GE SIGNA Hero Elite (China Only), Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA Voyager AIR (China Only), Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA PET/MR AIR Plus (China Only), Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA Hero MAX (China Only), Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA Architect AIR (China Only), Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Jul 30, 2025

SIGNA Architect

FDA Devices Moderate Jul 30, 2025

SIGNA Architect AIR

FDA Devices Moderate Jun 18, 2025

OEC Elite: The OEC Elite mobile C-arm is intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/device…

FDA Devices Moderate Apr 23, 2025

Venue Go Models: R2 (Model Number H45181VG), R3 (Model Number H45193VG), R4 (Model Number H45114VG), R5 (Model Numbers H45135VG, H45135VGW), R3 Surge…

FDA Devices Moderate Mar 19, 2025

GE Healthcare Revolution Apex, System, X-ray, Tomography, Computed

FDA Devices Moderate Mar 19, 2025

GE Healthcare Revolution Apex Select, System, X-ray, Tomography, Computed

FDA Devices Moderate Mar 19, 2025

GE Healthcare Revolution CT, System, X-ray, Tomography, Computed

FDA Devices Moderate Feb 12, 2025

Optima XR646 HD. X-Ray imaging system.

FDA Devices Moderate Feb 12, 2025

Definium 656HD & Discovery XR656HD (GTINs: 00840682138598, 00195278840226, 00840682136709). X-Ray imaging system.

FDA Devices Moderate Feb 12, 2025

Discovery XR656 HD. X-Ray imaging system.

FDA Devices Moderate Jan 22, 2025

Portrait Core Services, a set of software services that enable the communication and interaction of the Portrait Mobile Monitoring Solution component…

FDA Devices Moderate Jan 15, 2025

Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO

FDA Devices Moderate Jan 15, 2025

Tec 850 SEV Anesthesia Vaporizer, Reference Number 1177-9850-SEV

FDA Devices Moderate Jan 15, 2025

GE Healthcare Optima XR220amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-12; 2) 5555000-5; 3) 5555000-6; 4) A0659PB; 5…

FDA Devices Moderate Jan 15, 2025

GE Healthcare Optima XR200amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-3; 2) 5555000-4: 3) A0659MB

FDA Devices Moderate Jan 15, 2025

GE Healthcare Optima XR240amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-27; 2) 5555000-31; 3) 5555000-33; 4) 5555000-4…

FDA Devices Moderate Dec 4, 2024

SIGNA Architect AIR, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Dec 4, 2024

Discovery MR750w 3.0T, whole body magnetic resonance scanner

FDA Devices Moderate Dec 4, 2024

SIGNA Architect, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 14, 2024

SIGNA Explorer, with affected software versions: SV25.5, SV25.6, SV29.2, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 14, 2024

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…

FDA Devices Moderate Aug 14, 2024

SIGNA MR355, with affected software versions: SV25.5, SV25.6; Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 14, 2024

SIGNA PET/MR, with affected software versions: MP24.0, MP26.0, MP26.1, MR30.0, MR30.1; Tomographic imager combining emission computed tomography wit…

FDA Devices Moderate Aug 14, 2024

Discovery MR450 1.5T, with affected software versions: DV24.0, DV25.0, DV25.1, DV26.0; Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 14, 2024

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

FDA Devices Moderate Aug 14, 2024

Optima MR360, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 14, 2024

SIGNA UHP, with affected software versions: RX28.0, MR30.1; Nuclear Magnetic Resonance Imaging System - research use only

FDA Devices Moderate Aug 14, 2024

SIGNA MR380, with affected software versions: SV25.5, SV25.6; Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 14, 2024

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.

Compare GE Medical Systems, LLC with FORD →

Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds