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™ 500FA23HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 500DM25HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 505DA16HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 505DA20HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 505DA22HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 500DM27HEART-VALVE, MECHANICAL1 report
- SiteSeer™ 4A0029CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- SPRINTER® LEGEND SPL30020XCatheters, transluminal coronary angioplasty, percutaneous1 report
- SPRINTER® LEGEND SPL30015XCatheters, transluminal coronary angioplasty, percutaneous1 report
- SPRINTER® LEGEND SPL20020XCatheters, transluminal coronary angioplasty, percutaneous1 report
- SPRINTER® LEGEND SPL15012XCatheters, transluminal coronary angioplasty, percutaneous1 report
- SPRINTER® LEGEND SPL20006XCatheters, transluminal coronary angioplasty, percutaneous1 report
- SPRINTER® LEGEND SPL15015XCatheters, transluminal coronary angioplasty, percutaneous1 report
- SPRINTER® LEGEND SPL22512XCatheters, transluminal coronary angioplasty, percutaneous1 report
- ASSURANT® COBALT ASC860SVSTENT, ILIAC1 report
- ASSURANT® COBALT ASC930LVSTENT, ILIAC1 report
- ASSURANT® COBALT ASC960SVSTENT, ILIAC1 report
- SiteSeer™ 6A0082CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- SiteSeer™ 6A0001CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Pro-Flo™ 010028CATHETER, INTRAVASCULAR, DIAGNOSTIC1 death1 report
- SITESEER™ 06SR050CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- RF Marinr™ 075302Cardiac ablation percutaneous catheter1 report
- MEDTRONIC CARELINK EXPRESS™ 2020C1Pacemaker/icd/crt non-implanted components1 report
- Open Pivot™ 505DA16HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 500DM27HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 500DM31HEART-VALVE, MECHANICAL1 report
- DBS™ 3389S-28implanted subcortical electrical Stimulator (motor disorders)1 report
- Endurant® II ETBF3220C145ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1610C93ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1613C82ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETBF2813C124ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1628C156ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- Endurant® II ETLW1628C199ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1624C199ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- FREESTYLE® 995MS25heart-valve, non-allograft tissue1 report
- FREESTYLE® 995MS19heart-valve, non-allograft tissue1 report
- INPUT™ TS 091102AINTRODUCER, CATHETER1 report
- INPUT™ TS 051101AINTRODUCER, CATHETER1 report
- INPUT™ PS 050011INTRODUCER, CATHETER1 report
- INPUT™ TS 081102AINTRODUCER, CATHETER1 report
- EVEREST™ AC3200Syringe, balloon inflation1 report
- Injex™ 97792STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- Resolute Integrity™ RSINT30034UXCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT40018UXCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT40026UXCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT35034UXCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT25008UXCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT25012UXCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT27522UXCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT27530UXCoronary drug-eluting stent1 death1 report
- Resolute Integrity™ RSINT27508UXCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT27512UXCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT27518UXCoronary drug-eluting stent1 report
- Open Pivot™ 500DM25HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 500DM29HEART-VALVE, MECHANICAL1 report
- Open Pivot™ 500DM31HEART-VALVE, MECHANICAL1 report
- NA 8578PUMP, INFUSION, IMPLANTED, PROGRAMMABLE1 report
- NA 8596SCPUMP, INFUSION, IMPLANTED, PROGRAMMABLE1 report
- MEDTRONIC CARELINK EXPRESS™ 2020B2Pulse generator, permanent, implantable1 report
- NA ATLS04APPARATUS, AUTOTRANSFUSION1 report
- NA ATLS21APPARATUS, AUTOTRANSFUSION1 report
- Vectris™ SureScan® 977A160STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- NA 97740STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- Attain Command™ + SureValve™ 6250V-3DCATHETER, PERCUTANEOUS1 report
- Attain Command™ + SureValve™ 6250V-45SCATHETER, PERCUTANEOUS1 report
- Sentrant™ SENSH1428WINTRODUCER, CATHETER1 report
- Sentrant™ SENSH1828WINTRODUCER, CATHETER1 report
- COMPLETE® SE VASCULAR SC5100LVSTENT, SUPERFICIAL FEMORAL ARTERY1 report
- NA 3778-75STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- NA 3777-45STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- NA 3777-60STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- INDURA ® 1P 8709SCPUMP, INFUSION, IMPLANTED, PROGRAMMABLE1 report
- Simulus™ 800SC40RING, ANNULOPLASTY1 report
- Simulus™ 735AF37RING, ANNULOPLASTY1 report
- Simulus™ 700FF23RING, ANNULOPLASTY1 report
- Simulus™ 700FF39RING, ANNULOPLASTY1 report
- Cardioblate® CryoFlex® 60SF3Surgical Device, For cutting, coagulation, and/or ablation of tissue, including cardiac tissue1 report
- Tri-Ad™ 900SFC36RING, ANNULOPLASTY1 report
- Ascenda™ 8782PUMP, INFUSION, IMPLANTED, PROGRAMMABLE1 report
- Simulus™ 735AC35RING, ANNULOPLASTY1 report
- Nexframe® DB-2040Neurological stereotaxic Instrument1 report
- NA 3708260STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- NC SPRINTER® NCSP3027XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC SPRINTER® NCSP3512XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC SPRINTER® NCSP3515XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC SPRINTER® NCSP3527XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC SPRINTER® NCSP37515XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC SPRINTER® NCSP5015XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC SPRINTER® NCSP2021XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC SPRINTER® NCSP2521XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC SPRINTER® NCSP27515XCatheters, transluminal coronary angioplasty, percutaneous1 report
- NC SPRINTER® NCSP3015XCatheters, transluminal coronary angioplasty, percutaneous1 report
- Contegra® 200SH20pulmonic valved conduit1 report
- Contegra® 200SH16pulmonic valved conduit1 report
- Contegra® 200SH12pulmonic valved conduit1 report
- ATS Tri-Ad® 800SR24RING, ANNULOPLASTY1 report
- STREAMLINE™ 6494FELECTRODE, PACEMAKER, TEMPORARY1 report
- STREAMLINE™ 6500FELECTRODE, PACEMAKER, TEMPORARY1 report
- DBS ™ 3391S-40Deep brain stimulator for obsessive compulsive disorder (OCD)1 report
- NA 560BC1Control, pump speed, cardiopulmonary bypass1 report