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.
- VersaCross™ Access Solution VXSK0137Percutaneous atrial catheter kit1 recall0 reports
- VersaCross™ Transseptal Sheath VXS0201Introducer, catheter1 recall0 reports
- ENDOTAK RELIANCE® G 0177Implantable cardioverter defibrillator (non-CRT)1 recall0 reports
- PROPONENT™ SR L200Implantable pulse generator, pacemaker (non-CRT)1 recall0 reports
- LATITUDE® Clarity 7260Recorder, event, implantable cardiac, (with arrhythmia detection)1 recall0 reports
- LATITUDE® NXT 6460Pacemaker/icd/crt non-implanted components1 recall0 reports
- myLUX™ Patient App 2939Recorder, event, implantable cardiac, (with arrhythmia detection)1 recall0 reports
- IceRod® 1.5 i-Thaw® Cryoablation Needle FPRPR4009Unit, Cryosurgical, Accessories1 recall0 reports
- IceSeed® 1.5 MRI 90° Cryoablation Needle FPRPR3194Unit, Cryosurgical, Accessories1 recall0 reports
- IceSphere® 1.5 Cryoablation Needle FPRPR3558Unit, Cryosurgical, Accessories1 recall0 reports
- IceRod® i-Thaw® Prostate Cryoablation Kit / Visual-ICE® System FPRPR3572Unit, Cryosurgical, Accessories1 recall0 reports
- Guider Softip™ XF H965100420CATHETER, PERCUTANEOUS1 recall0 reports
- Guider Softip™ XF H965100460CATHETER, PERCUTANEOUS1 recall0 reports
- Guider Softip™ XF H965100470CATHETER, PERCUTANEOUS1 recall0 reports
- Guider Softip™ XF M003101430CATHETER, PERCUTANEOUS1 recall0 reports
- Guider Softip™ XF M003101460CATHETER, PERCUTANEOUS1 recall0 reports
- Guider Softip™ XF M003101470CATHETER, PERCUTANEOUS1 recall0 reports
- Expo™ H74908526051CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085261801CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085262021CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085262031CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Guider Softip™ XF M003100620CATHETER, PERCUTANEOUS1 recall0 reports
- Guider Softip™ XF M003100630CATHETER, PERCUTANEOUS1 recall0 reports
- Guider Softip™ XF M003101630CATHETER, PERCUTANEOUS1 recall0 reports
- UroMax Ultra Kit M0062251360DILATOR, URETHRAL1 recall0 reports
- UroMax Ultra Kit M0062251230DILATOR, URETHRAL1 recall0 reports
- UroMax Ultra Kit M0062251260DILATOR, URETHRAL1 recall0 reports
- UroMax Ultra Kit M0062251300DILATOR, URETHRAL1 recall0 reports
- UroMax Ultra Kit M0062251350DILATOR, URETHRAL1 recall0 reports
- Expo™ H74908526011CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H74908526041CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085261001CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085261711CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085261901CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085261951CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085262011CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085262201CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085262251CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085262301CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H74908526231CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085262351CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085262401CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H74908526241CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H74908526841CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H74908526861CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H74908526981CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H7490852620A1CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Capio RP M0068321010HOLDER, NEEDLE, GASTROENTEROLOGIC1 recall0 reports
- Expo™ H749085265001CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085265021CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314000CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314010CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314020CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314030CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314040CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314080CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314150CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314300CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314350CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314360CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314520CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314620CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314770CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314820CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314860CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- IMAGER™ II M001314880CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Rapid Refill M00566000SYRINGE, IRRIGATING (NON DENTAL)1 recall0 reports
- Hydratome RX 49 M00583000Unit, electrosurgical, endoscopic (with or without accessories)1 recall0 reports
- Contour VL™ M006180156180STENT, URETERAL1 recall0 reports
- Jagtome RX 44 M00573070Unit, electrosurgical, endoscopic (with or without accessories)1 recall0 reports
- Jagtome RX 49 M00573030Unit, electrosurgical, endoscopic (with or without accessories)1 recall0 reports
- Dreamtome™ RX 49 M00584020Unit, electrosurgical, endoscopic (with or without accessories)1 recall0 reports
- Carotid WALLSTENT® M001719000STENT, CAROTID1 recall0 reports
- MUSTANG™ H74939171080410CATHETER, BILIARY, DIAGNOSTIC50 reports
- Coyote™ H74939186351210CATHETER, PERCUTANEOUS1 recall0 reports
- Expo™ H74908526572A1CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H74908526573A1CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H74908526574A1CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H74908526575A1CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- ELUVIA™ H74939294601510Stent, superficial femoral artery, drug-eluting50 reports
- Expo™ H749085262501CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085262511CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085262521CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- Expo™ H749085262531CATHETER, INTRAVASCULAR, DIAGNOSTIC1 recall0 reports
- AngioJet® Ultra 5000A 105650-001HCATHETER, CORONARY, ATHERECTOMY1 recall0 reports
- AngioJet® Ultra 5000A 105650-001DCATHETER, CORONARY, ATHERECTOMY1 recall0 reports
- Comet H7493932440TRANSDUCER, PRESSURE, CATHETER TIP50 reports
- MAMBA™ H7493928713500CATHETER, PERCUTANEOUS1 recall0 reports
- Jagtome™ Revolution RX M00584250Unit, electrosurgical, endoscopic (with or without accessories)1 recall0 reports
- ORISE™ Gel M00519210Submucosal injection agent1 recall0 reports
- ORISE™ Gel M00519230Submucosal injection agent1 recall0 reports
- ORISE™ ProKnife M00519380Unit, electrosurgical, endoscopic (with or without accessories)1 recall0 reports
- ORISE™ ProKnife M00519400Unit, electrosurgical, endoscopic (with or without accessories)1 recall0 reports
- PERCIVA™ ICD DR D401Implantable cardioverter defibrillator (non-CRT)49 reports
- AMS 700 CX MS Pump 72404239Prosthesis, Penis, Inflatable49 reports
- AMS 700 LGX MS Pump 72404250Prosthesis, Penis, Inflatable49 reports
- Escape M0063902010DISLODGER, STONE, BASKET, URETERAL, METAL49 reports
- Quantum™ Maverick™ H7493808012270Catheters, transluminal coronary angioplasty, percutaneous1 death49 reports
- Ultraflex™ Esophageal NG M00513740PROSTHESIS, ESOPHAGEAL49 reports
- Jagwire M00556580Endoscopic guidewire, gastroenterology-urology1 death49 reports