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.
- Admiral™ Xtreme ADM050250130Catheter, angioplasty, peripheral, transluminal2 reports
- Admiral™ Xtreme ADM050300130LCatheter, angioplasty, peripheral, transluminal2 reports
- Admiral™ Xtreme ADM060250130LCatheter, angioplasty, peripheral, transluminal2 reports
- Pacific™ Plus PCP020040150Catheter, angioplasty, peripheral, transluminal2 reports
- Pacific™ Plus PCP060300150Catheter, angioplasty, peripheral, transluminal2 reports
- PACIFIC XTREME PCU040150130Catheter, angioplasty, peripheral, transluminal2 reports
- PACIFIC XTREME PCU040200130Catheter, percutaneous2 reports
- PACIFIC XTREME PCU050150130Catheter, angioplasty, peripheral, transluminal2 reports
- DLP® 69331Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 reports
- EOPA™ 77520Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 reports
- DLP® 10218CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 death2 reports
- DLP® 10014CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP® 10012CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP® 96428CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- TourniKwik™ 79011CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY2 reports
- DLP® 10051SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS2 reports
- DLP® 69324CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP® 94735CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP® 94745CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP® 89022CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- Select Series® 72122CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- Select Series® 73420CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP™ 77012Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 reports
- DLP™ 77016Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 reports
- DLP™ 77116Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 reports
- NA APU448INSTRUMENTS, SURGICAL, CARDIOVASCULAR2 reports
- EOPA™ 77618Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 death2 reports
- EOPA 3D® 78220Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 reports
- NA BB9L07R8Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- NA BB2W85R21Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- NA BB11P17R6Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- NA BB10Z66R12Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- NA BB7M47R9Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- NA BB9R01R23Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- NA BB4Q12R27Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- ACTIVA® Therapy 7482A51STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR1 report
- NA 3095-10Stimulator, electrical, implantable, for incontinence1 report
- NA 3777-60STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- NA 3777-75STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- Adapta™ ADVDD01Pulse generator, permanent, implantable1 report
- Capsure® VDD-2 5038S-58Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes1 report
- PISCES-QUAD 3487A-33STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- PISCES-QUAD 3487A-56STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- Capsurefix® Novus 407635permanent pacemaker Electrode1 report
- Capsurefix® Novus 407665permanent pacemaker Electrode1 death1 report
- ATTAIN COMMAND™ 6250S02CATHETER, PERCUTANEOUS1 report
- NA 37743STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- Intersept® XA6061TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- BIO-PUMP+® 95201PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 report
- PROFILE 3D™ 680R26RING, ANNULOPLASTY1 report
- Sprint Quattro Secure S™ DXAC/DSP 6935100permanent pacemaker Electrode1 report
- Sprint Quattro Secure S™ 6935100permanent pacemaker Electrode1 report
- SPECIFY 3998STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- BIO-MEDICUS® 96530-015CATHETER, PERCUTANEOUS1 report
- BIO-MEDICUS® 96530-017CATHETER, PERCUTANEOUS1 report
- BIO-MEDICUS® 96600-021CATHETER, PERCUTANEOUS1 report
- Bio-Medicus® 96670-019CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- Bio-Medicus® 96370-023CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- CG FUTURE® 638RL32RING, ANNULOPLASTY1 report
- CG FUTURE® 638BL38RING, ANNULOPLASTY1 report
- CG FUTURE® 638BL34RING, ANNULOPLASTY1 report
- CG FUTURE® 638BL28RING, ANNULOPLASTY1 report
- Duran AnCore® 620RG29RING, ANNULOPLASTY1 report
- Affinity® CB511OXYGENATOR, CARDIOPULMONARY BYPASS1 report
- Bio-Medicus® 96820-008CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- Bio-Medicus® 96820-012CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- Bio-Medicus® 96830-008CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- URCHIN® HP3500stabilizer,heart1 report
- RACER® BILIARY XD618YFCATHETER, BILIARY, DIAGNOSTIC1 report
- SPECIFY 39286-65STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- TALENT® OCCLUDER OCL18USSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- INDURA® 8709SCPUMP, INFUSION, IMPLANTED, PROGRAMMABLE1 report
- Contegra® 200SH12pulmonic valved conduit1 report
- INTERSTIM 3889-33Stimulator, electrical, implantable, for incontinence1 report
- Integrity INT30022WSTENT, CORONARY1 report
- NA 37744STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- NA 6719Permanent defibrillator electrodes1 report
- Affinity™ CP AP40PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 report
- Affinity™ CP CBAP40PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE1 report
- HANCOCK® II T510C31heart-valve, non-allograft tissue1 report
- NA 6G98RTUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- NA 3776-75STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- NA 3487A-56STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF1 report
- COMPLETE® SE VASCULAR SC720FVSTENT, ILIAC1 report
- COMPLETE® SE VASCULAR SC680LVSTENT, ILIAC1 report
- NA 355018STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF)1 report
- ATTAIN SELECT™ II 624890D02CATHETER, PERCUTANEOUS1 report
- ATTAIN SELECT™ II 6248DEL90DL02CATHETER, PERCUTANEOUS1 report
- NA 3550S-01COVER, BURR HOLE1 report
- Nexdrive™ MI-2000Neurological stereotaxic Instrument1 report
- DBS™ 3708640STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR1 report
- PROFILE 3D™ 680R28RING, ANNULOPLASTY1 report
- Duran AnCore® 620RG31RING, ANNULOPLASTY1 report
- Duran AnCore® 620RG27RING, ANNULOPLASTY1 report
- Duran AnCore® 620BG33RING, ANNULOPLASTY1 report
- Duran AnCore® 620BG29RING, ANNULOPLASTY1 report
- Duran AnCore® 620BG27RING, ANNULOPLASTY1 report
- Duran AnCore® 620BG25RING, ANNULOPLASTY1 report
- NA C315H4002CATHETER, PERCUTANEOUS1 report
- CG FUTURE® 638RL36RING, ANNULOPLASTY1 report