177 results
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22ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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GE Healthcare, Discovery XR656P/N 5374989/5397837 is intended to generate digital radiographic images of the skull, spinal column, chest, abdomen, extremities and other body parts in patients of all ages.
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·August 27, 2014
Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems
FDA Enforcement
Class II
·Terminated·GE Medical Systems, SCS·July 18, 2018
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 transmission projection data from the same axial plane taken at different angles.
FDA Enforcement
Class II
·Terminated·GE Medical Systems, LLC·December 16, 2015
GE Healthcare SIGNA Creator, SIGNA Explorer. Diagnostic Imaging Device.
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·September 14, 2016
NM/CT 850 Product Usage: The GE NM/CT 850 system is intended for general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body. It includes a general purpose Nuclear Medicine system using a variety of scanning modes supported by various acquisition types, and a Computed Tomography component which is intended specifically for enabling attenuation correction and anatomical localization of SPECT images.
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·May 8, 2019
Optima NM/CT 640 Product Usage: The GE Optima NM/CT 640 system is intended for General Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body. It includes a general purpose Nuclear Medicine (NM) system using a variety of scanning modes supported by various acquisition types, and a CT component which is intended specifically for enabling attenuation correction and anatomical localization on SPECT studies.
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·May 8, 2019
NM/CT 870 DR Product Usage: The GE Discovery NM/CT 670 system is a medical tool intended for use by appropriately trained health professionals to aid in detecting, localizing, diagnosing of diseases and organ function for the evaluation of diseases, trauma, abnormalities, and disorders such as, but not limited to, cardiovascular disease, neurological disorders and cancer. The system output can also be used by the physician for staging and restaging of tumors, planning, guiding, and monitoring therapy. The GE Discovery NM/CT 670 system, combining Nuclear Medicine (NM) and Computed Tomography (CT) systems, is intended to produce
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·May 8, 2019
Discovery NM 630 Product Usage: The Discovery NM 630 is an all-purpose dual detector nuclear imaging system intended for general nuclear medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using a variety of scanning modes supported by various acquisition types and imaging features designed to enhance image quality. The main components of the Discovery NM 630 system are: NM Gantry with Dual detector heads, patient table, Remote Control Unit and NM operation console.
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·May 8, 2019
Discovery IGS 740 Interventional Fluoroscopic X-ray Systems
FDA Enforcement
Class II
·Terminated·GE Medical Systems, SCS·July 18, 2018
NM/CT 860 Product Usage: The GE NM/CT 860 system is intended for general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body. It includes a general purpose Nuclear Medicine system using a variety of scanning modes supported by various acquisition types, and a Computed Tomography system which is intended for enabling attenuation correction and anatomical localization of SPECT images and for standalone head, whole body and vascular X-ray Computed Tomography applications.
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·May 8, 2019
Discovery NM/CT 670 DR Product Usage: The GE Discovery NM/CT 670 system is a medical tool intended for use by appropriately trained health professionals to aid in detecting, localizing, diagnosing of diseases and organ function for the evaluation of diseases, trauma, abnormalities, and disorders such as, but not limited to, cardiovascular disease, neurological disorders and cancer. The system output can also be used by the physician for staging and restaging of tumors, planning, guiding, and monitoring therapy. The GE Discovery NM/CT 670 system, combining Nuclear Medicine (NM) and Computed Tomography (CT) systems, is intended to produce:
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·May 8, 2019
Patient Circuit used with the Life Pulse High Frequency Ventilator. The Patient Circuit is a required disposable component of the Life Pulse High Frequency Ventilator. Model #(s): Individual Patient Circuit - catalog # 902 Patient Circuit Kit - catalog # 937: contains 2 circuits and 2 x 2.5 & 2 x 3.5 LifePort Adapters. Labeling states manufactured by: Bunnell Incorporated 436 Lawndale Drive, Salt Lake City, Utah 84115. Used for ventilating critically ill infants with pulmonary interstitial emphysema and infants with respiratory distress syndrome complicated by pulmonary air leaks, who are, in the opinion of their physicians, failing on conventional ventilation. The Patient Circuit is to provide a conduit for the humidification, warming, and temperature monitoring of the pressurized gas. The Patient Circuit is indicated for seven day single use.
FDA Recall
Terminated
·Bunnell, Inc.·Product code LSZ·November 19, 2012
Medtronic COMPLETE SE Self Expanding Biliary Stent System, Model number SC760L, includes a pre-loaded self-expanding Nickel-Titanium (Nitinol) stent with 8 tantalum radiopaque markers, 4 on each end, and an over the wire retractable sheath delivery system.
FDA Recall
Terminated
·Medtronic Cardiovascular·Product code FGE·November 24, 2008
GE Healthcare, CT Perfusion 4 on Advantage Workstation, CT and PET/CT consoles. Image analysis software package that allows the user to produce image data and to generate information with regard to changes in image intensity over time supporting CT Perfusion images.
FDA Recall
Terminated
·GE Medical Systems, LLC·Product code JAK·May 4, 2009
Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The SLIM handle is the grip for the SLIM driver in orthopedic surgical procedures.
FDA Enforcement
Class III
·Terminated·Pega Medical Inc.·May 27, 2020
HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753; 10C00200000 to 10C00210106 Product Usage: Samaritan 300/300P PAD is indicated for use on victims of sudden cardiac arrest who are exhibiting the following signs: Unconsciousness Not breathing Without circulation
FDA Enforcement
Class I
·Terminated·Heartsine Technologies, Limited·November 7, 2012
Accuprobe Group B Streptococcus Culture Identification Test, Catalog Number 2820B, Batch Number 531379, Gen-Probe, Incorporated, San Diego, CA. 92121
FDA Recall
Terminated
·Gen-Probe Inc·Product code MDK·May 2, 2007
Mycobacterium Tuberculosis Complex Culture Identification Test, 2860.
FDA Recall
Terminated
·Gen-Probe Inc·Product code LQF·December 30, 2008
Gen-Probe AccuProbe Group B Streptococcus Culture Identification Test Kit, 2820.
FDA Recall
Terminated
·Gen-Probe Inc·Product code MDK·December 30, 2008
Mycobacterium Avium Complex Culture Identification Test Identification Test Kit, 2835.
FDA Recall
Terminated
·Gen-Probe Inc·Product code LQF·December 30, 2008