Medtronic, Inc.
4,394 devices · 506,719 adverse event reports · 6,243 deaths reported · 1,396 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- SHERPA NX ACTIVE SA6CHAMP35CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL30CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL25CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL20SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL20ACATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL20CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL15SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL10SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL10DCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL10ACATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL10CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA63DRIGHTSHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA63DRIGHTCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA63DRCSHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA63DRCCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AR20SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AR20CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AR10SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AR10CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ALR12SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ALR12CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL75SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL75ACATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL75CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL40CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL30SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL30ACATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6IMASHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6IMADCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6IMACATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6HSISHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6HSIISHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6HSIIISHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6HSIIICATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6HSIICATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6HSICATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6FR40CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6FR35CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6FL40SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6JCR40CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6JCL40CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6JCL35CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6IMASHJCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ECR35CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6EBU50SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6EBU50CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6EBU45SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6FL40CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ERADRSTCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ERADRCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ERADLSTCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ERADLSHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ERADLLTCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ERADLCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ELGAMALSHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ELGAMALCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ECR40SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ECR40CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6ECR35SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6JR60SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL205CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6AL15CATHETER, PERCUTANEOUS1 recall0 reports
- NA CB6M85R7OXYGENATOR, CARDIOPULMONARY BYPASS1 recall0 reports
- INTERSEPT® 6T40R6TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- NA CB7D52ROXYGENATOR, CARDIOPULMONARY BYPASS1 recall0 reports
- NA TL6A65R7TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- NA CB6Z18R3OXYGENATOR, CARDIOPULMONARY BYPASS1 recall0 reports
- Contour 3D® 690R30RING, ANNULOPLASTY1 death50 reports
- Custom Perfusion System TL7C52R3PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- NA CB7J45R2OXYGENATOR, CARDIOPULMONARY BYPASS1 recall0 reports
- NA 6X37R6TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- Ascenda™ 8784PUMP, INFUSION, IMPLANTED, PROGRAMMABLE1 recall0 reports
- Custom Perfusion System 7T88RPUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- NA TL6C91R5TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- NA CB7N52ROXYGENATOR, CARDIOPULMONARY BYPASS1 recall0 reports
- NA CB7N54R1OXYGENATOR, CARDIOPULMONARY BYPASS1 recall0 reports
- NA HY6G55R9TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- Custom Perfusion System HY2K67R10PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- NA 7Y17R1TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- NA CB6V11R9OXYGENATOR, CARDIOPULMONARY BYPASS1 recall0 reports
- NA BB7P41R5TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- NA BB7P34R5TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- IN.PACT™ Admiral™ ADM05006013PDrug-Eluting Peripheral Transluminal Angioplasty Catheter1 recall0 reports
- NA HY3U59R13TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- NA HY3V10R27TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- Custom Perfusion System 6A30R1PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- NA CB5X49R17OXYGENATOR, CARDIOPULMONARY BYPASS1 recall0 reports
- NA BB1S56R19TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- NA BB8D73RTUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- MyCareLink™ 24950DPacemaker/icd/crt non-implanted components1 recall0 reports
- NA CB5D50R2OXYGENATOR, CARDIOPULMONARY BYPASS1 recall0 reports
- Custom Perfusion System HY1C33R26PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- Custom Perfusion System HY0Z20R21PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- Custom Perfusion System BB5Z97R14PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- Custom Perfusion System HY2800R37PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- Custom Perfusion System HY2J36R13PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- NA BB8F81RTUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- Endurant® II ETLW1620C124ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT4 deaths50 reports
- Custom Perfusion System BB7J04R9PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- NA BB4Q12R15TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports