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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Nitinol Smart and Smart Control Stent Implantation Systems CORDIS France ANSM
Exoseal Vascular Closure Device Cordis France ANSM
Nitinol SMART® CONTROL Endoprosthesis System Cordis® France ANSM
Powerflex Pro Peripheral Angioplasty Catheter Cordis France ANSM
Flexible Catheter for Circular Cartography Lasso BIOSENSE Webster INC;CORDIS SAS France ANSM
Nitinol Precise transhepatic biliary stents;Precision Nitinol Stent Insertion System CORDIS France ANSM
PTCA catheter batches CORDIS France ANSM
Device Recall Cordis POWERFLEX PRO PTA Dilatation Catheter Cardiovascular Devices Cordis Corporation 2 United States USFDA
Device Recall Cardinal Health Lubricated Intubating Stylet Anesthesiology Devices Cardinal Health 1 United States USFDA
Device Recall Ambitex NMD400 Nitrile Exam Gloves General Hospital and Personal Use Devices Cardinal Health 1 United States USFDA
Device Recall AVANTI Catheter Sheath Introducer System Cardiovascular Devices Cordis Corporation 2 United States USFDA
Device Recall Cardinal Health Gomco Style Circumcision Clamp Trays Obstetrical and Gynecological Devices Cardinal Health 2 United States USFDA
Device Recall MynxGrip Vascular Closure Device Cardiovascular Devices AccessClosure, Inc., A Cardinal Health Company 3 United States USFDA
Device Recall Arterial Blood Gas (ABG) Sampling Kit Anesthesiology Devices Cardinal Health 1 United States USFDA
Device Recall Cardinal Health BLUE IMPERVIOUS GOWN WITH THUMBHOOKS General Hospital and Personal Use Devices Cardinal Health 1 United States USFDA
Device Recall Converters(R) Under Buttocks Drape with Fluid Control Pouch II, General Hospital and Personal Use Devices Cardinal Health 200, LLC 2 United States USFDA
Device Recall Converters(R) Tiburon(R) Arthroscopy Drape General Hospital and Personal Use Devices Cardinal Health 200, LLC 2 United States USFDA
Device Recall Convertors Robotic Drape with Attached Leggings; Product is packaged as Single Sterile Drape Hematology and Pathology Devices Cardinal Health 200, LLC 1 United States USFDA
Device Recall MediVac(TM) Flex Advantage(TM) Suction Canister Liner General Hospital and Personal Use Devices Cardinal Health 200, LLC 2 United States USFDA
Device Recall Introducer guide Cardiovascular Devices Cordis Corporation 2 United States USFDA
Device Recall Guiding Catheter Cardiovascular Devices Cordis Corporation 2 United States USFDA
Product is a Powerflex P3 Dialation Catheter. Product is labeled in part: ''***POWERFLEX P3***Cordis***a Johnson and Johnson company***ENDOVASCULAR***STERILE EO***Cordis Europa N.V., 9301 LJ Roden, The Netherlands***'' Cardiovascular Devices Cordis Corporation 2 United States USFDA
Device Recall Diagnostic Catheter Cardiovascular Devices Cordis Corporation 2 United States USFDA
Device Recall CORDIS Peripheral Steerable Guidewire Cardiovascular Devices Cordis Corporation 2 United States USFDA
Device Recall CORDIS Peripheral Steerable Guidewire Cardiovascular Devices Cordis Corporation 2 United States USFDA