52 results · 30ms · Sources: EU EUDAMED, US FDA

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therascreen EGFR RGQ PCR Kit (24), Reference Number REF 870121

FDA Recall
Terminated ·Qiagen Sciences LLC·Product code OWG·April 8, 2020

OMG (Observational Mechanical Gateway) Connector - A Model Number SC-9305 The Precision Spinal Cord Stimulator System is indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs, including unilateral or bilateral pain associated with following: failed back surgery syndrome, intractable low back pain and leg pain. The Precision System includes an implantable l6-output, multi-channel stimulator (lPO - Implantable Pulse Generator) with a rechargeable battery power source. The lPG, commonly implanted in the abdomen or buttock area, can be configured to accept one or two leads. The leads are implanted in the epidural space, adjacent to the spinal column. The stimulation delivered at the distal end of the lead is intended to mask the pain signals.

FDA Recall
Terminated ·Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342·Product code LGW·April 22, 2008

Omega IV and Omega V tables on GE Innova 2100IQ Digital Fluoroscopic Imaging System

FDA Recall
Terminated ·GE Medical Systems, LLC·Product code MQB·December 22, 2009

Omega IV and Omega V tables on GE Innova 2000 fluoroscopic x-ray system

FDA Recall
Terminated ·GE Medical Systems, LLC·Product code MQB·December 22, 2009

Omega IV and Omega V tables on GE Innova 2121-1Q/3131--1Q Biplane Cardiovascular Imaging System.

FDA Recall
Terminated ·GE Medical Systems, LLC·Product code MQB·December 22, 2009

Omega IV and Omega V tables on GE Innova 4100/4100IQ GE Innova 4100 / 4100 IQ., x-ray system

FDA Recall
Terminated ·GE Medical Systems, LLC·Product code MQB·December 22, 2009

Omega IV and Omega V tables on GE Innova 3100/3100IQ GE Innova 3100 / 3100 IQ, Cardiovascular Imaging System

FDA Recall
Terminated ·GE Medical Systems, LLC·Product code MQB·December 22, 2009

Omega IV and Omega V tables on GE Advantx-E imaging system, used for general purpose diagnostic angiographic fluoroscopy and radiographic studies.

FDA Recall
Terminated ·GE Medical Systems, LLC·Product code MQB·December 22, 2009

GE, 1011-9000-000 Aisys Anesthesia Machine and Monitor

FDA Recall
Terminated ·Ge Healthcare, Llc·Product code BSZ·March 12, 2010

GE, 1009-9002-000 Avance Anesthesia Machine and Monitor

FDA Recall
Terminated ·Ge Healthcare, Llc·Product code BSZ·March 12, 2010

GE Centricity PACS (Picture Archiving and Communication System) RA1000 Workstation software; GE Healthcare Integrated IT Solutions, Barrington, IL 60010. The Centricity PACS is used to receive, store, distribute, display, manipulate, edit and annotate images throughout a clinical environment.

FDA Recall
Terminated ·GE Healthcare Integrated IT Solutions·Product code LLZ·September 25, 2009

GE Healthcare, Innova 2100IQ, Innova 3100IQ, Innova 4100IQ, Cardiovascular and Interventional Imaging System.

FDA Recall
Terminated ·GE Healthcare, LLC·Product code OWB·October 21, 2011

AMX Navigate Mobile X-Ray System

FDA Recall
Terminated ·GE Healthcare, LLC·Product code IZL·June 24, 2021

GE Signa Advantage nuclear magnetic resonance imaging system.

FDA Recall
Terminated ·GE Medical Systems, LLC·Product code LNH·August 19, 2005

GE Centricity PACS-IW software; GE Healthcare Integrated IT Solutions, Barrington, IL 60010. Device that receives, stores and communicates medical images and data from various imaging sources.

FDA Recall
Terminated ·Ge Healthcare It·Product code LLZ·February 11, 2010

GE Centricity Web Diagnostic (WebDX) software; GE Healthcare Integrated IT Solutions, Barrington, IL 60010. Device that receives, stores and communicates medical images and data from various imaging sources.

FDA Recall
Terminated ·Ge Healthcare It·Product code LLZ·February 11, 2010

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 of patients. The devices are intended for volume or pressure control ventilation.

FDA Recall
Terminated ·GE Medical Systems, LLC·Product code BSZ·December 15, 2015

GE Centricity Laboratory Instrument Interface software; GE Healthcare Integrated IT Solutions, Barrington, IL 60010. The intended use: the Centricity Laboratory is used to facilitate the general clinical, anatomic pathology and cytology laboratory workflow such as order entry, results entry, instrument interfacing, results reporting and patient record retrieval.

FDA Recall
Terminated ·Ge Healthcare It·Product code JQP·August 27, 2010

V-Probe, Endocare Cryo V Probe model # Cryo 206V. The product is used in a minimally invasive, percutaneous approach to treating prostate cancer in low, moderate and high risk patients. Prostate Cryoablation uses extremely cold temperatures to destroy cancerous tissue.

FDA Recall
Terminated ·Endocare, a Wholly Owned Subsidiary of HealthTronics, Inc.·Product code GEH·December 5, 2008

V-Probe, Endocare Cryo V Probe, single unit model # CVA2400. The product is used in a minimally invasive, percutaneous approach to treating prostate cancer in low, moderate and high risk patients. Prostate Cryoablation uses extremely cold temperatures to destroy cancerous tissue.

FDA Recall
Terminated ·Endocare, a Wholly Owned Subsidiary of HealthTronics, Inc.·Product code GEH·December 5, 2008