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.
- CG FUTURE® 638BL36RING, ANNULOPLASTY1 report
- CG FUTURE® 638BL32RING, ANNULOPLASTY1 report
- CG FUTURE® 638BL30RING, ANNULOPLASTY1 report
- CG FUTURE® 638BL28RING, ANNULOPLASTY1 report
- INTERSTIM® 3093-33Stimulator, electrical, implantable, for incontinence1 report
- INTERSTIM® 3889-41Stimulator, electrical, implantable, for incontinence1 report
- HANCOCK® II T505C229heart-valve, non-allograft tissue1 report
- ENDURANT® ENLW1628C93ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- ENDURANT® ENLW1628C82ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- ENDURANT® ENLW1620C82ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- ENDURANT® ENLW1613C82ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- ENDURANT® ENLW1610C124ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- ENDURANT® ENLW1610C93ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- ENDURANT® ENTF3636C70ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- ENDURANT® ENCF2525C49ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- ENDURANT® ENEW2828C82ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- ENDURANT® ENEW1313C82ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- ENDURANT® ENEW1010C82ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- ENDURANT® ENBF2516C124ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- ENDURANT® ENBF2513C145ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- ENDURANT® ENBF3220C145ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- HANCOCK II ULTRA® T505U221heart-valve, non-allograft tissue1 report
- HANCOCK II ULTRA® T505U227replacement Heart-valve1 report
- Launcher LA5ALR12CATHETER, PERCUTANEOUS1 report
- Resolute Integrity™ RSINT22514WCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT25030WCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT25014WCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT22518WCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT30018WCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT30015WCoronary drug-eluting stent1 report
- Resolute Integrity™ RSINT27512WCoronary drug-eluting stent1 report
- VALIANT® Captivia VAMC3838C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMC3232C100TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- VALIANT® Captivia VAMC2424C100TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- VALIANT® Captivia VAMF3838C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMF3434C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMF3232C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMF3838C200TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMF4040C200TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMF4444C200TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- Integrity INT35012UXSTENT, CORONARY1 report
- Integrity INT35015UXSTENT, CORONARY1 report
- Integrity INT35018UXSTENT, CORONARY1 report
- Integrity INT35030UXSTENT, CORONARY1 report
- Integrity INT40015UXSTENT, CORONARY1 report
- Integrity INT40018UXSTENT, CORONARY1 death1 report
- Integrity INT22508UXSTENT, CORONARY1 report
- Integrity INT22514UXSTENT, CORONARY1 report
- Integrity INT22526UXSTENT, CORONARY1 report
- Integrity INT27514UXSTENT, CORONARY1 report
- Integrity INT27522UXSTENT, CORONARY1 report
- Integrity INT27526UXSTENT, CORONARY1 report
- VALIANT® Captivia VAMC2824C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- VALIANT® Captivia VAMC4238C150TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- Z2 Z27EBU35CATHETER, PERCUTANEOUS1 report
- Z2 Z26EBU375CATHETER, PERCUTANEOUS1 report
- Z2 Z26EBU35CATHETER, PERCUTANEOUS1 report
- Z2 Z26FR40CATHETER, PERCUTANEOUS1 report
- Z2 ZM5JL30CATHETER, PERCUTANEOUS1 report
- Z2 ZM5AL10CATHETER, PERCUTANEOUS1 report
- Z2 ZM5AR20CATHETER, PERCUTANEOUS1 report
- Launcher LA6JR40SHCATHETER, PERCUTANEOUS1 report
- Launcher LA6JR50SHCATHETER, PERCUTANEOUS1 report
- Launcher LA6JR405CATHETER, PERCUTANEOUS1 report
- Launcher LA6MAC3030CATHETER, PERCUTANEOUS1 report
- Launcher LA6JL30CATHETER, PERCUTANEOUS1 report
- Launcher LA6RCBSHCATHETER, PERCUTANEOUS1 report
- Launcher LA6RDCKCATHETER, PERCUTANEOUS1 report
- Launcher LA6SAL10SHCATHETER, PERCUTANEOUS1 report
- Launcher LA6RBU35CATHETER, PERCUTANEOUS1 report
- Launcher LA6AR20SHCATHETER, PERCUTANEOUS1 report
- Launcher LA6AL15CATHETER, PERCUTANEOUS1 report
- Launcher LA63DRCCATHETER, PERCUTANEOUS1 report
- Launcher LA6AR20CATHETER, PERCUTANEOUS1 report
- Launcher LA6FR40CATHETER, PERCUTANEOUS1 report
- Launcher LA6EBU40CATHETER, PERCUTANEOUS1 report
- Launcher LA6ERADRCATHETER, PERCUTANEOUS1 report
- SHERPA NX BALANCED SB6EBU375CATHETER, PERCUTANEOUS1 report
- SHERPA NX BALANCED SB6EBU35CATHETER, PERCUTANEOUS1 report
- SHERPA NX BALANCED SB6AL20CATHETER, PERCUTANEOUS1 report
- TAIGA TA6JR40CATHETER, PERCUTANEOUS1 report
- TAIGA TA6EBU35CATHETER, PERCUTANEOUS1 report
- TAIGA TA6AL10CATHETER, PERCUTANEOUS1 report
- Launcher LA7MAC35CATHETER, PERCUTANEOUS1 report
- Launcher LA7JL35SHCATHETER, PERCUTANEOUS1 report
- Launcher LA7JL35CATHETER, PERCUTANEOUS1 report
- Launcher LA7RDCKCATHETER, PERCUTANEOUS1 report
- Launcher LA7AL75CATHETER, PERCUTANEOUS1 report
- SHERPA NX BALANCED SB7JL40SHCATHETER, PERCUTANEOUS1 report
- SHERPA NX BALANCED SB7JL35SHCATHETER, PERCUTANEOUS1 report
- SHERPA NX BALANCED SB7EBU30CATHETER, PERCUTANEOUS1 report
- SHERPA NX BALANCED SB7AL10SHCATHETER, PERCUTANEOUS1 report
- SHERPA NX BALANCED SB7EBU40SHCATHETER, PERCUTANEOUS1 report
- DBS™ 3755INSTRUMENT, SURGICAL, NON-POWERED1 report
- Contour 3D™ 690R30RING, ANNULOPLASTY1 report
- Contour 3D™ 690R32RING, ANNULOPLASTY1 report
- Contour 3D™ 690R36RING, ANNULOPLASTY1 report
- SiteSeer™ 4A0025CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- NA 37651STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS1 report
- Open Pivot™ 500FA21HEART-VALVE, MECHANICAL1 report