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.
- Open Pivot™ 502AG25HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 502AG27HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 501DM26HEART-VALVE, MECHANICAL1 death1 report
- Open Pivot™ 500FA21HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 500FA23HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 500FA27HEART-VALVE, MECHANICAL1 report
- VALIANT® Captivia VAMC4444C200TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- VALIANT® Captivia VAMC3030B100TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMC2626C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMC4642C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMC4040C200TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMC3228C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMC3026C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- VALIANT® Captivia VAMF2424C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMF2222C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- VALIANT® Captivia VAMC4242C100TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- VALIANT® Captivia VAMC3636C100TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMC3434C100TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMC3030C100TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- VALIANT® Captivia VAMC2828C100TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMC4242B100TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMC3434B100TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- NA 203CXCardiac ablation percutaneous catheter1 report
- IN.PACT™ Admiral™ ADM06012013PDrug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- IN.PACT™ Admiral™ ADM04004008PDrug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- IN.PACT™ Admiral™ ADM04012008PDrug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- IN.PACT™ Admiral™ ADM05006008PDrug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- IN.PACT™ Admiral™ ADM06004008PDrug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- NC Euphora™ NCEUP32520XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC Euphora™ NCEUP32512XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC Euphora™ NCEUP27512XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC Euphora™ NCEUP2508XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC Euphora™ NCEUP4520XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC Euphora™ NCEUP5015XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC Euphora™ NCEUP27506XCatheters, transluminal coronary angioplasty, percutaneous1 death1 report
- NC Euphora™ NCEUP2527XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC Euphora™ NCEUP4006XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC Euphora™ NCEUP37520XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC Euphora™ NCEUP2020XCatheters, transluminal coronary angioplasty, percutaneous1 report
- CareLink® Monitor 2490G23Pacemaker/icd/crt non-implanted components1 report
- NA 5846VImplantable pulse generator, pacemaker (non-CRT)1 report
- THUNDER® THNDR190JWIRE, GUIDE, CATHETER1 report
- ZINGER® LIGHT LVZRLS180JWIRE, GUIDE, CATHETER1 report
- ATTAIN HYBRID™ Guide Wire GWR419578WIRE, GUIDE, CATHETER1 report
- ATTAIN HYBRID™ Guide Wire GWR419488WIRE, GUIDE, CATHETER1 report
- COUGAR® XT CGRXT190JWIRE, GUIDE, CATHETER1 report
- ProVia 9 9PROV300HSWIRE, GUIDE, CATHETER1 report
- COUGAR® LS LVCLS190JWIRE, GUIDE, CATHETER1 report
- CARELINK® MONITOR 2490G24Pulse generator, permanent, implantable1 report
- Endurant® II ETLW1628C82ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Adapta® ADVDD01Pulse generator, permanent, implantable1 report
- NA 8578PUMP, INFUSION, IMPLANTED, PROGRAMMABLE1 report
- NA 8731SCPUMP, INFUSION, IMPLANTED, PROGRAMMABLE1 report
- NA 2037ACardiac ablation percutaneous catheter1 report
- Flexcath® Advance 4FC12CATHETER, STEERABLE1 report
- Freezor® 307F3Cardiac ablation percutaneous catheter1 report
- Arctic Front® 2AF234Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation1 report
- Freezor® MAX 239F5Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation1 report
- Freezor® Xtra 227F5Cardiac ablation percutaneous catheter1 report
- NA 97740STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- NA 37651STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR1 report
- DBS 3389S-28implanted subcortical electrical Stimulator (motor disorders)1 report
- NA 97740STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- NA 37642STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS1 report
- NA 97754STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- Custom Perfusion System HY7W83R4PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 report
- HANCOCK® II T510C27replacement Heart-valve1 report
- SPRINT QUATTRO SECURE S™ DXAC/DSP 6935100permanent pacemaker Electrode1 report
- SPRINT QUATTRO SECURE® DXAC/DSP 6947100Permanent defibrillator electrodes1 report
- CAPSUREFIX® NOVUS 4076110permanent pacemaker Electrode1 report
- Resolute Onyx™ RONYX50026UXCoronary drug-eluting stent1 report
- Ascenda® 8785PUMP, INFUSION, IMPLANTED, PROGRAMMABLE1 report
- N/A PA96000DETECTOR AND ALARM, ARRHYTHMIA1 report
- ATTAIN® BIPOLAR OTW 419478permanent pacemaker Electrode1 report
- ATTAIN STARFIX™ 419578Drug eluting permanent left ventricular (lv) pacemaker electrode1 report
- CAPSURE®SP NOVUS 5092-58permanent pacemaker Electrode1 report
- HANCOCK II ULTRA® T505U221replacement Heart-valve1 death1 report
- HANCOCK II ULTRA® T505U227replacement Heart-valve1 report
- HANCOCK II ULTRA® T505U221replacement Heart-valve1 report
- HANCOCK II ULTRA® T505U227replacement Heart-valve1 report
- MOSAIC ULTRA® 305U219heart-valve, non-allograft tissue1 report
- Resolute Onyx™ RONYX20012WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX20018WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX22508WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX22518WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX22522WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX25008WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX25026WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX25030WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX27512WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX27522WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX27526WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX30034WCoronary drug-eluting stent1 report
- Resolute Onyx™ RONYX40022WCoronary drug-eluting stent1 report
- PlasmaBlade(TM) PS200-040-SPELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- Bio-Medicus™ 96820-112CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- Bio-Medicus™ 96830-108CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- PlasmaBlade PS200-001ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- NA BB8V10R2TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- CAPSURE® Z NOVUS 5054-52permanent pacemaker Electrode1 report