Abbott Vascular Inc.
1,126 devices · 52,399 adverse event reports · 516 deaths reported · 25 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.
- NC TREK NEO™ 1400275-20Catheters, transluminal coronary angioplasty, percutaneous1 report
- NC TREK NEO™ 1400375-20Catheters, transluminal coronary angioplasty, percutaneous1 report
- NC TREK NEO™ 1400450-15Catheters, transluminal coronary angioplasty, percutaneous1 report
- NC TREK NEO™ 1400500-20Catheters, transluminal coronary angioplasty, percutaneous1 report
- XIENCE Skypoint™ 1804325-08Coronary drug-eluting stent1 report
- XIENCE Skypoint™ 1804325-33Coronary drug-eluting stent1 report
- XIENCE Skypoint™ 1804450-15Coronary drug-eluting stent1 report
- XIENCE Skypoint™ 1804450-28Coronary drug-eluting stent1 report
- XIENCE Skypoint™ 1804500-12Coronary drug-eluting stent1 report
- XIENCE Skypoint™ 1804500-18Coronary drug-eluting stent1 death1 report
- Supera™ S-75-100-120-P6STENT, SUPERFICIAL FEMORAL ARTERY1 report
- Supera™ S-70-030-120-P6STENT, SUPERFICIAL FEMORAL ARTERY1 report
- Esprit™Scaffold, infrapopliteal, absorbable1 report
- XACT™ 83025-01STENT, CAROTID1 report
- XACT™ 83023-01STENT, CAROTID1 report
- XACT™ 83027-01STENT, CAROTID1 report
- HI-TORQUE COMMAND™ 1060001Wire, guide, catheter1 report
- HI-TORQUE COMMAND™ 1060002Wire, guide, catheter1 report
- HI-TORQUE COMMAND™ 1060004AWire, guide, catheter1 report
- Esprit™ 1203300-18Scaffold, Infrapopliteal, Absorbable1 report
- Esprit™ 1203375-28Scaffold, Infrapopliteal, Absorbable1 report
- Esprit™ 1203250-18Scaffold, Infrapopliteal, Absorbable1 report
- SUPERA S-45-040-120-P6STENT, SUPERFICIAL FEMORAL ARTERY1 report
- SUPERA S-65-100-120-P6STENT, SUPERFICIAL FEMORAL ARTERY1 report
- SUPERA S-45-030-120-P6STENT, SUPERFICIAL FEMORAL ARTERY1 report
- SUPERA S-65-020-120-P6STENT, SUPERFICIAL FEMORAL ARTERY1 report