Boston Scientific Corporation
4,038 devices · 274,337 adverse event reports · 2,107 deaths reported · 451 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.
- Coyote™ H74939186251090CATHETER, PERCUTANEOUS1 report
- Coyote™ H74939186350810CATHETER, PERCUTANEOUS1 report
- Coyote™ H74939186350890CATHETER, PERCUTANEOUS1 report
- Coyote™ H74939186400610CATHETER, PERCUTANEOUS1 report
- Coyote™ H74939186400810CATHETER, PERCUTANEOUS1 report
- Coyote™ H74939186351510CATHETER, PERCUTANEOUS1 report
- Coyote™ H74939185251010Catheter, angioplasty, peripheral, transluminal1 report
- Coyote™ H74939185300810Catheter, angioplasty, peripheral, transluminal1 report
- Coyote™ H74939186251290CATHETER, PERCUTANEOUS1 report
- Coyote™ H74939186301590CATHETER, PERCUTANEOUS1 report
- Coyote™ H74939186350610CATHETER, PERCUTANEOUS1 report
- Coyote™ H74939186401210CATHETER, PERCUTANEOUS1 report
- OffRoad™ H74939202100540Catheter for crossing total occlusions1 report
- V-14™ Control Wire™ H74939216918220WIRE, GUIDE, CATHETER1 report
- WallFlex™ Biliary Transhepatic M00574690CATHETER, BILIARY, DIAGNOSTIC1 report
- WallFlex™ Biliary Transhepatic M00574720CATHETER, BILIARY, DIAGNOSTIC1 report
- WallFlex™ Biliary Transhepatic M00574740CATHETER, BILIARY, DIAGNOSTIC1 report
- WallFlex™ Biliary Transhepatic M00574710CATHETER, BILIARY, DIAGNOSTIC1 report
- WallFlex™ Biliary Transhepatic M00574630CATHETER, BILIARY, DIAGNOSTIC1 report
- WallFlex™ Biliary Transhepatic M00574650CATHETER, BILIARY, DIAGNOSTIC1 report
- Ascerta™ M0061456120STENT, URETERAL1 report
- Ascerta™ M0061456190STENT, URETERAL1 report
- Ascerta™ M0061456210STENT, URETERAL1 report
- Blazer Prime® HTD M004P5031THK20Cardiac ablation percutaneous catheter1 report
- Charger™ H74939206100270CATHETER, BILIARY, DIAGNOSTIC1 report
- Charger™ H74939206100410CATHETER, BILIARY, DIAGNOSTIC1 report
- Charger™ H74939206031010CATHETER, BILIARY, DIAGNOSTIC1 report
- Charger™ H74939206041010CATHETER, BILIARY, DIAGNOSTIC1 report
- Charger™ H74939206041810Catheter, angioplasty, peripheral, transluminal1 report
- Charger™ H74939206040410Catheter, angioplasty, peripheral, transluminal1 report
- Charger™ H74939206040470Catheter, angioplasty, peripheral, transluminal1 report
- Charger™ H74939206040810Catheter, angioplasty, peripheral, transluminal1 report
- Charger™ H74939206051510CATHETER, BILIARY, DIAGNOSTIC1 report
- Charger™ H74939206050470CATHETER, BILIARY, DIAGNOSTIC1 report
- Charger™ H74939206061070CATHETER, BILIARY, DIAGNOSTIC1 report
- Charger™ H74939206061210CATHETER, BILIARY, DIAGNOSTIC1 report
- Charger™ H74939206060270Catheter, angioplasty, peripheral, transluminal1 report
- Charger™ H74939206060410CATHETER, BILIARY, DIAGNOSTIC1 report
- Charger™ H74939206060470CATHETER, BILIARY, DIAGNOSTIC1 report
- Charger™ H74939206090470Catheter, angioplasty, peripheral, transluminal1 report
- Epic™ Vascular H74939200103020STENT, ILIAC1 report
- Epic™ Vascular H74939200123070STENT, ILIAC1 report
- Epic™ Vascular H74939200064020STENT, ILIAC1 report
- Epic™ Vascular H74939200066070STENT, ILIAC1 report
- Epic™ Vascular H74939200071220STENT, ILIAC1 report
- Epic™ Vascular H74939200071270STENT, ILIAC1 report
- Epic™ Vascular H74939200076070STENT, ILIAC1 report
- Epic™ Vascular H74939200083020STENT, ILIAC1 report
- Epic™ Vascular H74939200092020STENT, ILIAC1 report
- Epic™ Vascular H74939200093020STENT, ILIAC1 report
- Epic™ Vascular H74939200094020STENT, ILIAC1 report
- Epic™ Vascular H74939200096020STENT, ILIAC1 report
- Emerge™ Push H7493919012120Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ Push H7493919015120Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493918915220Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493918915400Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493918920120Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493918920270Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493918920350Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493918920400Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493918908350Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493919115120Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493919115400Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493919120120Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493919120150Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493919130220Catheters, transluminal coronary angioplasty, percutaneous1 report
- Emerge™ H7493919108120Catheters, transluminal coronary angioplasty, percutaneous1 report
- PROMUS Element™ Plus H7493911612250Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911616250Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911620250Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911612270Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911628270Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911608300Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911616350Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911628350Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911420220Coronary drug-eluting stent1 death1 report
- PROMUS Element™ Plus H7493911432220Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911420250Coronary drug-eluting stent1 death1 report
- PROMUS Element™ Plus H7493911424250Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911408250Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911416270Coronary drug-eluting stent1 death1 report
- PROMUS Element™ Plus H7493911424270Coronary drug-eluting stent1 death1 report
- PROMUS Element™ Plus H7493911424350Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911428350Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911412400Coronary drug-eluting stent1 report
- PROMUS Element™ Plus H7493911416400Coronary drug-eluting stent1 death1 report
- PROMUS Element™ Plus H7493911408400Coronary drug-eluting stent1 death1 report
- Flextome® Cutting Balloon® H749CBM3200060Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring1 report
- Flextome® Cutting Balloon® H749CBM3375060Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring1 report
- Flextome® Cutting Balloon® H749CBM3400060Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring1 report
- Flextome® Cutting Balloon® H749CBM3250150Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring1 report
- Flextome® Cutting Balloon® H749CBO3400150Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring1 report
- Gladiator™ Elite H74939207030440Catheter, angioplasty, peripheral, transluminal1 report
- Gladiator™ Elite H74939207040870Catheter, angioplasty, peripheral, transluminal1 report
- Gladiator™ Elite H74939207050270Catheter, angioplasty, peripheral, transluminal1 report
- Gladiator™ Elite H74939207050870Catheter, angioplasty, peripheral, transluminal1 report
- Gladiator™ Elite H74939207060270Catheter, angioplasty, peripheral, transluminal1 report
- Gladiator™ Elite H74939207080440Catheter, angioplasty, peripheral, transluminal1 report
- iLab Ultrasound Imaging System H749ILAB120INS0COMPUTER, DIAGNOSTIC, PROGRAMMABLE1 report
- ION™ H7493902432250Coronary drug-eluting stent1 report