Catheter, cannula and tubing, vascular, cardiopulmonary bypass

FDA product code DWF · Class 2 · 813 devices · 1,796 reports · 41 deaths reported · 383 devices named in recalls

• EOPA 3D® 78220

  Medtronic, Inc. · CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS
  1 report
• EOPA 3D® 78222

  Medtronic, Inc. · CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS
  1 report
• NA DLP3D76R1

  Medtronic, Inc. · CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS
  1 report
• DLP™ 77108

  Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass
  1 report
• EOPA 3D® 78322

  Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass
  1 report
• EOPA™ 77518

  Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass
  1 report
• EOPA™ 77724

  Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass
  1 report
• DLP™ 77012

  Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass
  1 report
• DLP™ 77210

  Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass
  1 report
• EOPA™ 77622

  Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass
  1 report
• EOPA 3D® 78222

  Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass
  1 report
• CLEARVIEW® 31225

  Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass
  1 report
• AngioDynamics 25184

  Navilyst Medical, Inc. · CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS
  1 report