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.
- ONCOZENE® 06-0301-01003-02Device, Vascular, for Promoting Embolization1 report
- TRUEtome™ Revolution 39 M00583260Unit, electrosurgical, endoscopic (with or without accessories)1 report
- TRUEtome™ Revolution 44 M00583270Unit, electrosurgical, endoscopic (with or without accessories)1 report
- Tria™ Soft M0061903430Stent, ureteral1 report
- Tria™ Soft M0061903440Stent, ureteral1 report
- Jagwire™ Revolution M00557010Endoscopic guidewire, gastroenterology-urology1 report
- CRE™ RX M00558910CATHETER, BILIARY, DIAGNOSTIC1 report
- RHYTHMIA HDx™ M004RH1020R0COMPUTER, DIAGNOSTIC, PROGRAMMABLE1 report
- ZelanteDVT™ ClotHunter™ 114690-001Catheter, continuous flush1 death1 report
- RHYTHMIA HDx™ M004RH20020COMPUTER, DIAGNOSTIC, PROGRAMMABLE1 report
- SYNERGY™ H7493926032500Coronary drug-eluting stent1 report
- Athletis™ H74939347060410Catheter, angioplasty, peripheral, transluminal1 report
- Athletis™ H74939347070450Catheter, angioplasty, peripheral, transluminal1 report
- Athletis™ H74939347080850Catheter, angioplasty, peripheral, transluminal1 report
- Athletis™ H74939347120670Catheter, angioplasty, peripheral, transluminal1 report
- JUDO™ 3 H749393773000Wire, guide, catheter1 report
- Ranger™ H74939419702010Drug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- TRUSELECT™ M001394101050Catheter, continuous flush1 report
- TRUSELECT™ M001394111750Catheter, continuous flush1 report
- LithoVue Empower™ M0067919900Adaptor, Bulbs, Miscellaneous, For Endoscope1 report
- Flexiva Pulse M006L8405940Powered laser surgical instrument1 report
- VENOUS WALLSTENT™ H74912044106870Stent, iliac vein1 report
- VENOUS WALLSTENT™ H74912044149070Stent, iliac vein1 report
- VENOUS WALLSTENT™ H74912044164070Stent, iliac vein1 report
- Ultra ICE™ Plus - PI H7493932800990Echocardiograph1 report
- EMBOLD™ Fibered M001394240050080Device, Vascular, for Promoting Embolization1 report
- EMBOLD™ Fibered M001394240060100Device, Vascular, for Promoting Embolization1 report
- SYNERGY MEGATRON™ H7493942808350Coronary drug-eluting stent1 report
- SYNERGY MEGATRON™ H7493942808400Coronary drug-eluting stent1 report
- SYNERGY MEGATRON™ H7493942808450Coronary drug-eluting stent1 report
- SYNERGY MEGATRON™ H7493942812400Coronary drug-eluting stent1 report
- SYNERGY MEGATRON™ H7493942824450Coronary drug-eluting stent1 report
- SYNERGY MEGATRON™ H7493942828400Coronary drug-eluting stent1 death1 report
- SYNERGY MEGATRON™ H7493942828450Coronary drug-eluting stent1 report
- EndoArmor™ Plus SGE-389-10Non-surgical isolation gown1 report
- Direxion™ HI-FLO™ Fathom™-16 System M001195960Catheter, continuous flush1 report
- SMARTFREEZE™ M004CRBS400Z0Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation1 report
- SpyGlass™ Discover M0054295R0Led light source1 report