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.
- WallFlex™ Biliary M00570510CATHETER, BILIARY, DIAGNOSTIC1 report
- Interlock™ M001361750Device, Vascular, for Promoting Embolization1 report
- Polaris™ Loop M0061552110STENT, URETERAL1 report
- Polaris™ Loop M006155223090STENT, URETERAL1 report
- Percuflex™ Plus M006175253190STENT, URETERAL1 report
- Contour VL™ M006180155170STENT, URETERAL1 report
- Polaris™ Ultra M006192133170STENT, URETERAL1 report
- Coyote™ ES H74939135203010Catheter, angioplasty, peripheral, transluminal1 report
- Coyote™ ES H74939135253010Catheter, angioplasty, peripheral, transluminal1 report
- Coyote™ ES H74939135303010Catheter, angioplasty, peripheral, transluminal1 report
- Coyote™ ES H74939135353010Catheter, angioplasty, peripheral, transluminal1 report
- Coyote™ ES H74939135354010Catheter, angioplasty, peripheral, transluminal1 report
- Coyote™ ES H74939134203010Catheter, angioplasty, peripheral, transluminal1 report
- Coyote™ ES H74939134352010Catheter, angioplasty, peripheral, transluminal1 report
- Coyote™ ES H74939134402010Catheter, angioplasty, peripheral, transluminal1 report
- OptiFlex M0063903000DISLODGER, STONE, BASKET, URETERAL, METAL1 report
- Percuflex™ Plus M006175253180STENT, URETERAL1 report
- Percuflex™ Plus M006175263190STENT, URETERAL1 report
- Xenform™ M0068302410Mesh, surgical1 report
- RunWay™ H74938969686B0CATHETER, PERCUTANEOUS1 report
- Percuflex™ M006145352190STENT, URETERAL1 report
- Polaris™ Ultra M006192133180STENT, URETERAL1 report
- Stretch™ VL M006185155180TUBE, DRAINAGE, SUPRAPUBIC1 report
- Polaris™ Ultra M006192134010STENT, URETERAL1 report
- Polaris™ Ultra M006192133010STENT, URETERAL1 report
- Dreamwire M00556120STYLET FOR CATHETER, GASTRO-UROLOGY1 report
- Blazer™ Dx-20 M00420SL2520CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING1 report
- Blazer™ Dx-20 M00420SL2820CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING1 report
- Sterling® SL H74939148258010CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939148351010CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939148351210CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939148201090CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939148251090CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939148251290CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939148251590CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939148301290CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939148308090CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939148351590CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939148401290CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939147201010Catheter, angioplasty, peripheral, transluminal1 report
- Sterling® SL H74939147301010Catheter, angioplasty, peripheral, transluminal1 report
- Sterling® SL H74939147301510Catheter, angioplasty, peripheral, transluminal1 report
- Sterling® SL H74939147308010CATHETER, PERCUTANEOUS1 report
- Sterling® SL H74939147358010Catheter, angioplasty, peripheral, transluminal1 report
- NC Quantum Apex™ H7493912406270Catheters, transluminal coronary angioplasty, percutaneous1 report
- NC Quantum Apex™ H7493912408320Catheters, transluminal coronary angioplasty, percutaneous1 report
- NC Quantum Apex™ H7493912408370Catheters, transluminal coronary angioplasty, percutaneous1 report
- NC Quantum Apex™ H7493912408500Catheters, transluminal coronary angioplasty, percutaneous1 report
- NC Quantum Apex™ H7493912415220Catheters, transluminal coronary angioplasty, percutaneous1 report
- NC Quantum Apex™ H7493912420200Catheters, transluminal coronary angioplasty, percutaneous1 report
- NC Quantum Apex™ H7493912420500Catheters, transluminal coronary angioplasty, percutaneous1 report
- NC Quantum Apex™ H7493912430200Catheters, transluminal coronary angioplasty, percutaneous1 report
- NC Quantum Apex™ H7493912430320Catheters, transluminal coronary angioplasty, percutaneous1 report
- Polaris™ Ultra M006192132050STENT, URETERAL1 report
- Advanix™ Biliary M00533250CATHETER, BILIARY, DIAGNOSTIC1 report
- Advanix™ Biliary M00533350CATHETER, BILIARY, DIAGNOSTIC1 report
- Advanix™ Biliary M00533370CATHETER, BILIARY, DIAGNOSTIC1 report
- Advanix™ Biliary M00532870CATHETER, BILIARY, DIAGNOSTIC1 report
- Advanix™ Biliary M00532890CATHETER, BILIARY, DIAGNOSTIC1 report
- Advanix™ Biliary M00532950CATHETER, BILIARY, DIAGNOSTIC1 report
- Advanix™ Biliary M00532990CATHETER, BILIARY, DIAGNOSTIC1 report
- Advanix™ Biliary M00533010CATHETER, BILIARY, DIAGNOSTIC1 report
- Advanix™ Biliary M00532230CATHETER, BILIARY, DIAGNOSTIC1 report
- Advanix™ Biliary M00532240CATHETER, BILIARY, DIAGNOSTIC1 report
- Advanix™ Biliary M00534620CATHETER, BILIARY, DIAGNOSTIC1 report
- Advanix™ Biliary M00534660CATHETER, BILIARY, DIAGNOSTIC1 report
- EndoVive Jejunal Feeding Tube M00566330TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Journey™ M001391260WIRE, GUIDE, CATHETER1 report
- Journey™ M001391270WIRE, GUIDE, CATHETER1 report
- Extractor™ Pro RX M00547040CATHETER, BILIARY, DIAGNOSTIC1 report
- Renegade™ HI-FLO™ FATHOM™ System M001184500Catheter, continuous flush1 report
- Renegade™ HI-FLO™ FATHOM™ System M001184520Catheter, continuous flush1 report
- Renegade™ HI-FLO™ FATHOM™ System M001184530Catheter, continuous flush1 report
- Gateway® M0032072215300intracranial neurovascular stent1 report
- Gateway® M0032072215250intracranial neurovascular stent1 report
- Interlock™-35 M001363700Device, Vascular, for Promoting Embolization1 report
- MUSTANG™ H74939171070210CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171051270CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171030270CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171082010Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171081510Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171030210CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171082070Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171051810Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171070370CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171070240CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171100370CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171081270CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171081570Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171071810Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171100840CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171031070CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171050840CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171090640CATHETER, BILIARY, DIAGNOSTIC1 report
- Interlock™-35 M001363910Device, Vascular, for Promoting Embolization1 report
- Coyote™ H74939185200610CATHETER, PERCUTANEOUS1 report
- Coyote™ H74939185200810Catheter, angioplasty, peripheral, transluminal1 report
- Coyote™ H74939185300610Catheter, angioplasty, peripheral, transluminal1 report
- Coyote™ H74939186200890CATHETER, PERCUTANEOUS1 report
- Coyote™ H74939186201290CATHETER, PERCUTANEOUS1 report