Manufacturer

GE Medical Systems, LLC

168 recalls in our database name GE Medical Systems, LLC as the manufacturing or recalling firm.

What the numbers show

Total: 168
Critical: 0
Severe: 4
Most recent: 2026-07-22

Of the 168 recalls from GE Medical Systems, LLC we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 4 (2%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

151–168 of 168

ModerateFDA (Devices)·Z-1049-2016·2016-03-16
GE Medical Systems Recalls CT and PET CT Scanners for Incorrect Torque Values
GE Medical Systems is recalling 817 CT and PET CT scanner systems worldwide because service manuals contained incorrect torque values.
Product
Discovery LS, 2286327 LightSpeed 4.0 CT Scanner System - The LightSpeed 4.0 CT Scanner System is indicated for head and whole body X-ray Computed Tomography applications. PET Discovery ST system - The GE Discovery ST system is intended for head and whole body attenuation corre
Category
Medical Device
Distribution
4 states
LowFDA (Devices)·Z-1052-2016·2016-03-16
GE Medical Systems Recalls CT and PET CT Scanners for Manual Error
GE Medical Systems is recalling specific CT and PET CT scanners because service manuals contained an incorrect torque value.
Product
LightSpeed Plus (4-slice MDAS LightSpeed 4.0 CT Scanner System - The LightSpeed 4.0 CT Scanner System is indicated for head and whole body X-ray Computed Tomography applications. PET Discovery ST system - The GE Discovery ST system is intended for head and whole body attenuation
Category
Medical Device
Distribution
4 states
LowFDA (Devices)·Z-1048-2016·2016-03-16
GE Medical Systems Recalls CT and PET CT Scanners for Service Manual Error
GE Medical Systems is recalling 25 CT and PET CT scanner systems because their service manuals contain an incorrect torque value.
Product
LightSpeed Ultra (8-slice MDAS), 5120327-3 LightSpeed 4.0 CT Scanner System - The LightSpeed 4.0 CT Scanner System is indicated for head and whole body X-ray Computed Tomography applications. PET Discovery ST system - The GE Discovery ST system is intended for head and whole b
Category
Medical Device
Distribution
4 states
LowFDA (Devices)·Z-1053-2016·2016-03-16
GE Medical Systems Recalls CT and PET Scanners for Incorrect Torque Values
GE Medical Systems is recalling 104 CT and PET/CT scanners worldwide because service manuals contained incorrect torque values.
Product
LightSpeed QX/I (4-slice MDAS) LightSpeed 4.0 CT Scanner System - The LightSpeed 4.0 CT Scanner System is indicated for head and whole body X-ray Computed Tomography applications. PET Discovery ST system - The GE Discovery ST system is intended for head and whole body attenuat
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0768-2016·2016-02-17
GE Healthcare Optima XR220amx Mobile Radiographic System Recalled for Safety Latch Failure
GE Medical Systems is recalling 2,389 Optima XR220amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.
Product
GE Healthcare, Optima XR220amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0763-2016·2016-02-17
GE Medical Systems Recalls Mavig Monitor Suspension System Due to Fall Risk
GE Medical Systems is recalling 2,111 Mavig Monitor Suspension Systems because a reported incident involved a suspension arm falling to the floor.
Product
Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+, Advantx LCN+, Advantx LCLP+, Advantx LCA, INNOVA 2000, INNOVA 4100, INNOVA 3100, INNOVA 3131IQ, INNOVA 2121IQ, INNOVA 2100IQ, INNOVA 3100IQ, and INNOVA 4100IQ
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0770-2016·2016-02-17
GE Healthcare Optima XR200amx Mobile Radiographic System Recalled for Safety Latch Failure
GE Medical Systems is recalling 895 Optima XR200amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.
Product
GE Healthcare, Optima XR200amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0769-2016·2016-02-17
GE Brivo XR285amx Mobile Radiographic System Recalled for Safety Latch Failure
GE Medical Systems is recalling 126 Brivo XR285amx mobile radiographic systems worldwide because a safety latch mechanism may fail, posing a risk of bodily harm.
Product
GE Healthcare, Brivo XR285amx Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
Category
Medical Device
Distribution
4 states
SevereFDA (Devices)·Z-0677-2016·2016-01-27
GE Aespire Anesthesia Systems Recalled for Potential Barotrauma Risk
GE Medical Systems is recalling Aespire 7900 and Aespire View anesthesia systems because a stuck valve could cause excessive pressure and barotrauma.
Product
GE Healthcare, Aespire 7900, 1009-9012-000 & Aespire View, 1009-9212-000. The family of GE Datex-Ohmeda Aespire anesthesia systems with 7900 ventilator (Aespire 7900 and Aespire View) is intended to provide general inhalation anesthesia and ventilatory support to a wide range
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0680-2016·2016-01-27
GE Aisys Anesthesia System Recalled for Potential Barotrauma Risk
GE Medical Systems is recalling 13 Aisys Anesthesia Systems because a stuck valve could cause excessive pressure in the patient breathing circuit, potentially resulting in barotrauma.
Product
GE Healthcare, Aisys, 1011-9000-000. The GE Datex-Ohmeda Aisys Anesthesia System is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonatal, pediatric, adult). The device is intended for volume or pressure control ventila
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0678-2016·2016-01-27
GE Healthcare Aestiva 7900 Ventilator Recall for Stuck Valve Risk
GE Medical Systems is recalling two Aestiva 7900 ventilators because a stuck valve could cause excessive pressure and barotrauma.
Product
GE Healthcare, Aestiva 7900, 1006-9305-000. This version of the Datex-Ohmeda 7900 ventilator is used in Datex-Ohmeda Aestiva/5 anesthesia systems. It is a microprocessor based, electronically controlled, pneumatically driven ventilator that provides patient ventilation during su
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0679-2016·2016-01-27
GE Healthcare Aestiva MRI Ventilator Recalled for Valve Defect
GE Medical Systems is recalling 84 Aestiva MRI anesthesia systems because a drive gas check valve may become stuck open, potentially causing excessive pressure in the patient breathing circuit.
Product
GE Healthcare, Aestiva MRI, 1006-9310-000. This version of the Datex-Ohmeda 7900 ventilator is used in Datex-Ohmeda Aestiva/5 anesthesia systems. It is a microprocessor based, electronically controlled, pneumatically driven ventilator that provides patient ventilation during sur
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0681-2016·2016-01-27
GE Healthcare Anesthesia Systems Recalled for Potential Barotrauma Risk
GE Medical Systems is recalling certain Aisys and Avance anesthesia systems because a stuck valve could cause excessive pressure in the patient breathing circuit, potentially leading to barotrauma.
Product
GE Healthcare, Aisys CS2,1011-9050-000; Avance Amingo,1009-9002-000, & Avance CS2, 1009-9050-000. The GE Datex-Ohmeda Aisys Anesthesia System is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonatal, pediatric, adult). T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0682-2016·2016-01-27
GE Medical Systems Recalls Anesthesia Device Service Kits Due to Valve Defect
GE Medical Systems is recalling 240 anesthesia device service kits because a drive gas check valve could become stuck open, potentially causing excessive pressure in the patient breathing circuit.
Product
Anesthesia device service kits. ASSY-MSN, VENT ENGINE ASSY, 1503-8101-000 ASSY-MSN, VENT ENGINE ASSY 7900, 1009-8216-000 ASSY-MSN, VENT ENGINE ASSY AESPIRE 7900 1009-8423-000 ASSY-MSN, VENT ENGINE ASSY, AESTIVA 7900 MRI 1503-8102-000 ASSY-MSN, VLV ASSY DR GAS CHK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0413-2016·2015-12-23
GE Healthcare Recalls Optima CL323i and IGS 320 X-ray Systems
GE Healthcare is recalling 108 Optima CL323i and Optima IGS 320 angiographic X-ray systems due to a potential loss of displayed imaging.
Product
GE Healthcare Optima CL323i Product Usage: The angiographic X-ray systems are indicated for use for patients from newborn to geriatric in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular and non-vascular, diagnostic and intervention
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0414-2016·2015-12-23
GE Healthcare Optima IGS 320 Recall for Loss of Displayed Imaging
GE Medical Systems is recalling 45 Optima IGS 320 systems due to a potential safety issue involving non-recoverable loss of displayed imaging.
Product
GE Healthcare Optima IGS 320. Product Usage: The angiographic X-ray systems are indicated for use for patients from newborn to geriatric in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular and non-vascular, diagnostic and interventio
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0401-2016·2015-12-16
GE Revolution CT Scanners Recalled for Potential Head Scan Artifacts
GE Medical Systems is recalling 125 Revolution CT scanners worldwide due to potential image artifacts in head scans that may mimic pathology. No injuries have been reported.
Product
GE Healthcare, Revolution CT Scanners. Revolution CT- The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. The system is intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmissi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0196-2016·2015-11-11
GE Recalls MR Surgical Suite II Tables Due to Transfer Mechanism Issue
GE Medical Systems is recalling MR Surgical Suite II Tables because a defect in the transfer release mechanism may prevent patient transfer between the MR and surgical tables.
Product
MR Surgical Suite II Table, Model Number(s): M8074SS, M8053SS, M0074SS. UPDATE 11-4-2015: Model M0001SS
Category
Medical Device
Distribution
8 states

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

GE Medical Systems Global Technology

R&D Subsidiary of GE Healthcare

Country: United States
Parent company: GE HealthCare

Source: Wikidata (Q21168536), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.