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.
- NA BB9N31R3Pump, blood, cardiopulmonary bypass, non-roller type1 recall1 report
- Valiant Navion™ VNMF2525C185TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 recall1 death1 report
- Valiant Navion™ VNMF3125C173TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 recall1 report
- Cardioblate® CryoFlex® 60SF7Surgical Device, For cutting, coagulation, and/or ablation of tissue, including cardiac tissue1 recall1 report
- SelectSecure™ MRI SureScan™ 383074permanent pacemaker Electrode1 death51 reports
- NA BB7Y33R8Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- IN.PACT™ AV IAV06008008PDrug-coated peripheral transluminal angioplasty catheter1 recall1 report
- Confida™ CES122230INTRODUCER, CATHETER1 recall1 report
- NA BB10R94R6Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA BB8L80R5Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- Valiant Navion™ VNMF2828C174TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 recall1 report
- Valiant Navion™ VNMF3131C174TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 recall1 report
- Valiant Navion™ VNMF3434C174TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 recall1 report
- Valiant Navion™ VNMF4040C183TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 recall1 death1 report
- Valiant Navion™ VNMF4343C183TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 recall1 report
- Valiant Navion™ VNMF4337C185TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 recall1 report
- Valiant Navion™ VNMC4337C200TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 recall1 report
- NA BB8X02R9Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- N/A 2035UCardiac ablation percutaneous catheter1 recall1 report
- NA HY10J00R6Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 death1 report
- NA BB10E61R4Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA BB10Q99R11Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA HY11G55R1Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA BB7U03R21Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA BB10B05R15Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA BB9L88R22Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA HY8C67R16Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA BB9H96R3Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA HY11P20R4Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA HY9M86R11Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA BB11G87R3Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA BB11T08R1Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA HY11U75R2Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA BB8E21R13Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA HY7X82R12Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA BB11U86R5Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA BB4Q12R19Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NanoCross™ Elite AB14W050040150Catheter, angioplasty, peripheral, transluminal1 recall1 report
- NanoCross™ Elite AB14W050060150Catheter, angioplasty, peripheral, transluminal1 recall1 report
- NanoCross™ Elite AB14W050120150Catheter, angioplasty, peripheral, transluminal1 recall1 report
- NanoCross™ Elite AB14W060080150Catheter, angioplasty, peripheral, transluminal1 recall1 report
- NA BB7Q27R10Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- EOPA™ 77522Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- DLP® 12002CATHETER, STEERABLE1 recall1 report
- DLP® 66132CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- DLP® 69320CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- DLP® 67318CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- DLP® 68128CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- DLP® 68120CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- VC2™ 93448CCATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- MC2® 91246CCATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- DLP® 12118CATHETER, STEERABLE1 recall1 report
- DLP® 94215TCATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- DLP® 94725CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- MC2® 91228CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- DLP® 80220CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- DLP® 80222CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- Select Series® 72120CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 recall1 report
- DLP® 12115Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- DLP™ 77006Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall1 report
- NA CB4Z27ROXYGENATOR, CARDIOPULMONARY BYPASS1 recall0 reports
- INTERSEPT® 2D25R6TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- NA 5B54R3TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- INTERSEPT® 2R88R3TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- Custom Perfusion System TL5V70R1PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- Custom Perfusion System TL5U46R2PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- NA CB5S68R3OXYGENATOR, CARDIOPULMONARY BYPASS1 recall0 reports
- NA TL4F88R7TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- Custom Perfusion System CB2E68R6PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- NA TL6C89R1TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- Intersept® Custom Tubing Pack 1N16R19PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- Custom Perfusion System TL5V78R4PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- Custom Perfusion System TL5U45R3PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- NA TL2T88R10TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- Custom Perfusion System CB6M65RPUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 recall0 reports
- Nexprobe™ NP-1000Neurological stereotaxic Instrument1 recall0 reports
- MOSAIC ULTRA® 305U225heart-valve, non-allograft tissue50 reports
- SHERPA NX ACTIVE SA6LCBSHDCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6LCBSHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6LCBDCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6LCBCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MAC30CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MAC3030CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MAC30SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MAC35CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6LARACATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6JR60CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6JR50SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6JR50CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6JR45SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6JR45CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6JR40SHACATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MP1SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MP1KCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MP1CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MB2SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MB2CATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MB1SHCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MB1DCATHETER, PERCUTANEOUS1 recall0 reports
- SHERPA NX ACTIVE SA6MB1CATHETER, PERCUTANEOUS1 recall0 reports