3,450 results
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14ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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CORDIS "Dura Star" 2.25 x 25 Dilatation Catheter, Catalog # 70125225, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
CORDIS "Fire Star" 3.50 x 10 Dilatation Catheter, Catalog # 80110350, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
Cordis EMPIRA RX PTCA Dilatation Catheter
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·June 23, 2014
Boston Scientific Cutting Balloon Ultra2 Monorail Device, Boston Scientific, One Boston Scientific Place, Natick, MA 01760.
FDA Recall
Terminated
·Boston Scientific·Product code LOX·July 21, 2006
Euphora Rapid Exchange Balloon Dilatation Catheter, a Percutaneous Transluminal Coronary Angioplasty (PTCA) Rapid Exchange System.
FDA Recall
Terminated
·Medtronic Vascular Galway DBA Medtronic Ireland Parkmore Business Park West Galway Ireland·Product code LOX·July 13, 2017
NC TREK Coronary Dilatation Catheter, REF 1012455-120 Rx Only,NC TREK RX 5.00 X 20MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated for: a) balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving myocardial perfusion b) balloon dilatation of a coronary artery occlusion, for the purpose of restoring coronary flow in patients with ST-segment elevation myocardial infarction c) balloon dilatation of a stent after implantation (balloon models 2.00 mm 5.00 mm only)
FDA Recall
Terminated
·Abbott Vascular·Product code LOX·January 29, 2020
NC TRAVELER Coronary Dilatation Catheter, REF 1013157-15, Rx Only,NC Traveler RX 4.0 X 15MM The NC Traveler RX Coronary Dilatation Catheter is not cleared for commercial distribution in the United States.
FDA Recall
Terminated
·Abbott Vascular·Product code LOX·January 29, 2020
CORDIS "Dura Star" 3.50 x 15 Dilatation Catheter, Catalog # 70115350, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
CORDIS "Fire Star" 2.25 x 10 Dilatation Catheter, Catalog # 80110225, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
CORDIS "Dura Star" 4.00 x 15 Dilatation Catheter, Catalog # 70115400, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
CORDIS "Dura Star" 3.25 x 15 Dilatation Catheter, Catalog # 70115325, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
CORDIS "Fire Star" 1.50 x 20, Single Marker Band, Dilatation Catheter, Catalog # 8012015S, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
CORDIS "Dura Star" 3.75 x 25 Dilatation Catheter, Catalog # 70125375, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
CORDIS "Dura Star" 2.75 x 25 Dilatation Catheter, Catalog # 70125275, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
CORDIS "Dura Star" 2.75 x 15 Dilatation Catheter, Catalog # 70115275, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
CORDIS "Dura Star" 2.50 x 10 Dilatation Catheter, Catalog # 70110250, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
CORDIS "Dura Star" 3.25 x 25 Dilatation Catheter, Catalog # 70125325, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
CORDIS "Dura Star" 3.00 x 10 Dilatation Catheter, Catalog # 70110300, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall
Terminated
·Cordis Corporation·Product code LOX·January 14, 2008
Boston Scientific Scimed Maverick 2 Monorail" PTCA Catheter, 3.0 mm 15 mm REF 38928-1530 Lot 9565194 Use before 2010-04 Indicated for balloon dilation of the stenotic portion of a coronary artery or bypass graft stenosis for the purpose of improving myocardial perfusion.
FDA Recall
Terminated
·Boston Scientific Corporation One Boston·Product code LOX·May 1, 2007
NC TREK Coronary Dilatation Catheter, REF 1012453-20 Rx Only, NC TREK RX 4.50 X 8MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated for: a) balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving myocardial perfusion b) balloon dilatation of a coronary artery occlusion, for the purpose of restoring coronary flow in patients with ST-segment elevation myocardial infarction c) balloon dilatation of a stent after implantation (balloon models 2.00 mm 5.00 mm only)
FDA Recall
Terminated
·Abbott Vascular·Product code LOX·January 29, 2020