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.

• ATTAIN SELECT™ II 6248130D02

  CATHETER, PERCUTANEOUS
  2 reports
• Duran AnCore® 620BG35

  RING, ANNULOPLASTY
  2 reports
• CG FUTURE® 638RL30

  RING, ANNULOPLASTY
  2 reports
• Duran AnCore® 620RG23

  RING, ANNULOPLASTY
  2 reports
• ENDURANT® ENLW1616C93E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• ENDURANT® ENLW1616C82E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• ENDURANT® ENLW1613C93E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  1 death2 reports
• ENDURANT® ENEW2424C82E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• ENDURANT® ENLW1628C124E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• ENDURANT® ENBF2813C166E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  1 death2 reports
• ENDURANT® ENBF2813C145E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  1 death2 reports
• ENDURANT® ENBF3620C145E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• ENDURANT® ENBF3220C166E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• ENDURANT® ENBF3216C124E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• ENDURANT® ENBF2820C166E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• HANCOCK II ULTRA® T505U225

  heart-valve, non-allograft tissue
  2 reports
• Launcher LA5JR40

  CATHETER, PERCUTANEOUS
  2 reports
• NA 6707-15

  permanent pacemaker Electrode
  2 reports
• VALIANT® Captivia VAMF4040C150TU

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  1 death2 reports
• VALIANT® Captivia VAMF3636C200TU

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  1 death2 reports
• Integrity INT30015UX

  STENT, CORONARY
  2 reports
• Integrity INT30022UX

  STENT, CORONARY
  2 reports
• Integrity INT35022UX

  STENT, CORONARY
  2 reports
• Integrity INT40009UX

  STENT, CORONARY
  2 reports
• Integrity INT22512UX

  STENT, CORONARY
  2 reports
• Integrity INT22522UX

  STENT, CORONARY
  2 reports
• Launcher LA6JR35SH

  CATHETER, PERCUTANEOUS
  2 reports
• Launcher LA6MP1SH

  CATHETER, PERCUTANEOUS
  2 reports
• Launcher LA6MB2

  CATHETER, PERCUTANEOUS
  2 reports
• Launcher LA6EBU355

  CATHETER, PERCUTANEOUS
  2 reports
• Launcher LA6AL10

  CATHETER, PERCUTANEOUS
  2 reports
• Launcher LA6IMA

  CATHETER, PERCUTANEOUS
  2 reports
• Launcher LA6EBU35SH

  CATHETER, PERCUTANEOUS
  2 reports
• Launcher LA6EBU375

  CATHETER, PERCUTANEOUS
  2 reports
• Launcher LA6ERADL

  CATHETER, PERCUTANEOUS
  2 reports
• Launcher LA7EBU35

  CATHETER, PERCUTANEOUS
  2 reports
• SHERPA NX BALANCED SB7EBU375SH

  CATHETER, PERCUTANEOUS
  2 reports
• Contour 3D™ 690R28

  RING, ANNULOPLASTY
  2 reports
• Contour 3D™ 690R34

  RING, ANNULOPLASTY
  2 reports
• Open Pivot™ 500DM33

  HEART-VALVE, MECHANICAL
  2 reports
• Open Pivot™ 500DM29

  HEART-VALVE, MECHANICAL
  2 reports
• SPRINTER® LEGEND SPL25020X

  Catheters, transluminal coronary angioplasty, percutaneous
  2 reports
• INTERSTIM® 305901

  Stimulator, electrical, implantable, for incontinence
  2 reports
• N/A 97745

  STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
  2 reports
• Open Pivot™ 500DM33

  HEART-VALVE, MECHANICAL
  2 reports
• Open Pivot™ 501DM24

  HEART-VALVE, MECHANICAL
  1 death2 reports
• Endurant® II ETLW1610C124E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• Endurant® II ETLW1610C156E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• Endurant® II ETLW1613C124E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• Endurant® II ETLW1613C156E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• Endurant® II ETLW1624C93E

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• FREESTYLE® 995CS21

  heart-valve, non-allograft tissue
  2 reports
• FREESTYLE® 995CS25

  heart-valve, non-allograft tissue
  2 reports
• INPUT™ TS 051102A

  INTRODUCER, CATHETER
  2 reports
• INPUT™ PS 060011

  INTRODUCER, CATHETER
  2 reports
• Resolute Integrity™ RSINT35009UX

  Coronary drug-eluting stent
  2 reports
• Resolute Integrity™ RSINT35015UX

  Coronary drug-eluting stent
  2 reports
• Resolute Integrity™ RSINT40030UX

  Coronary drug-eluting stent
  2 reports
• Resolute Integrity™ RSINT40038UX

  Coronary drug-eluting stent
  2 reports
• Resolute Integrity™ RSINT35038UX

  Coronary drug-eluting stent
  2 reports
• Resolute Integrity™ RSINT40009UX

  Coronary drug-eluting stent
  1 death2 reports
• Resolute Integrity™ RSINT22508UX

  Coronary drug-eluting stent
  1 death2 reports
• Resolute Integrity™ RSINT27526UX

  Coronary drug-eluting stent
  2 reports
• Resolute Integrity™ RSINT30009UX

  Coronary drug-eluting stent
  2 reports
• PULSAR®II PS100-102RF

  ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
  2 reports
• Sprint Quattro Secure® 6947M97

  permanent pacemaker Electrode
  2 reports
• CARELINK® MONITOR 2490G21

  Pulse generator, permanent, implantable
  2 reports
• CARELINK® MONITOR 2490H9

  Pulse generator, permanent, implantable
  2 reports
• NA 97754

  STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
  2 reports
• NA 37754

  STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
  2 reports
• Attain Command™ + SureValve™ 6250V-MPX

  CATHETER, PERCUTANEOUS
  2 reports
• Attain Command™ + SureValve™ 6250V-EHXL

  CATHETER, PERCUTANEOUS
  2 reports
• Attain Command™ + SureValve™ 6250VC

  CATHETER, PERCUTANEOUS
  2 reports
• Sentrant™ SENSH2428W

  INTRODUCER, CATHETER
  2 reports
• NA 3777-45

  STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
  2 reports
• Affinity Fusion® BB841

  RESERVOIR, BLOOD, CARDIOPULMONARY BYPASS
  2 reports
• Simulus™ 800SC38

  RING, ANNULOPLASTY
  2 reports
• Simulus™ 800SC26

  RING, ANNULOPLASTY
  2 reports
• Simulus™ 700FF37

  RING, ANNULOPLASTY
  2 reports
• Simulus™ 700FF35

  RING, ANNULOPLASTY
  2 reports
• Attain Select™ II + SureValve™ 6248V-90SP

  CATHETER, PERCUTANEOUS
  2 reports
• MEDTRONIC CARELINK® MONITOR 2490C15

  Pulse generator, permanent, implantable
  2 reports
• autoLog® ATLG110

  APPARATUS, AUTOTRANSFUSION
  2 reports
• SPRINTER® LEGEND SPL12506X

  Catheters, transluminal coronary angioplasty, percutaneous
  2 reports
• SPRINTER® LEGEND SPL12512X

  Catheters, transluminal coronary angioplasty, percutaneous
  2 reports
• NA 3708240

  STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
  2 reports
• Selectsecure™ 383074

  Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes
  2 reports
• Contegra® 200SH14

  pulmonic valved conduit
  2 reports
• Contegra® 200H18

  pulmonic valved conduit
  2 reports
• NA 5846V

  Implantable pulse generator, pacemaker (non-CRT)
  2 reports
• STREAMLINE™ 6492F

  ELECTRODE, PACEMAKER, TEMPORARY
  2 reports
• CARELINK® MONITOR 2490H10

  Pacemaker/icd/crt non-implanted components
  2 reports
• Open Pivot™ 505DA26

  HEART-VALVE, MECHANICAL
  2 reports
• Open Pivot™ 505DA16

  HEART-VALVE, MECHANICAL
  1 death2 reports
• Open Pivot™ 500DM31

  HEART-VALVE, MECHANICAL
  2 reports
• VALIANT® Captivia VAMC3030C150TU

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  1 death2 reports
• VALIANT® Captivia VAMC2828C150TU

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• VALIANT® Captivia VAMC4646C100TU

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• VALIANT® Captivia VAMC3434C200TU

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports
• VALIANT® Captivia VAMC3636C150TU

  SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
  2 reports