PlainRecalls

Ge Medical Systems, LLC

Compiled from official public sources by the editorial team.

157 recalls on record · Latest: May 20, 2026

Ge Medical Systems, LLC Recall Insight

Ge Medical Systems, LLC appears on 157 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.154% 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 May 20, 2026, 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 Mar 19, 2025 to May 20, 2026.

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 May 20, 2026

Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15

FDA Devices Moderate May 20, 2026

Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300

FDA Devices Moderate May 20, 2026

Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27

FDA Devices Moderate May 20, 2026

Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23

FDA Devices Moderate May 20, 2026

Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20

FDA Devices Moderate May 20, 2026

Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25

FDA Devices Moderate May 20, 2026

Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6

FDA Devices Moderate Apr 1, 2026

Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LP

FDA Devices Moderate Mar 25, 2026

Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from va…

FDA Devices Moderate Mar 25, 2026

Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data fro…

FDA Devices Moderate Mar 25, 2026

Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from var…

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 Oct 22, 2025

LOGIQ P10 series with software version R4.5.7 Model Number 5877534

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 Aug 20, 2025

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

FDA Devices Moderate Aug 20, 2025

GE SIGNA Architect, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE Discovery MR750w 3.0T, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA Premier, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE Optima MR450w 1.5T, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA UHP, Nuclear Magnetic Resonance Imaging System

FDA Devices Moderate Aug 20, 2025

GE SIGNA Hero, 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 Jul 30, 2025

SIGNA PET/MR

FDA Devices Moderate Jul 30, 2025

Discovery MR750w 3.0T

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 Jun 18, 2025

OEC 3D

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 Apr 23, 2025

Venue Fit Models: R3 (Model Number H45303VFSC, H45303VFSW), R4 (Model Number H45314VFS, H45314VFSW), Venue Fit R5 system (Model Numbers H45335VFS, H4…

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

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Ge Medical Systems, LLC with Zimmer Biomet, Inc. →

Data Sources

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.