Terumo Cardiovascular Systems Corporation
317 devices · 3,562 adverse event reports · 30 deaths reported · 183 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.
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- Cardiovascular Procedure Kit 71064-01Laparoscope, General & Plastic Surgery1 recall0 reports
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- Cardiovascular Procedure Kit 76498Laparoscope, General & Plastic Surgery1 recall0 reports
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- Terumo® Advanced Perfusion System 1 5791Console, Heart-Lung Machine, Cardiopulmonary Bypass1 recall0 reports
- Terumo® Advanced Perfusion System 1 217390Console, Heart-Lung Machine, Cardiopulmonary Bypass1 recall0 reports
- Capiox® FX Advance Hollow Fiber Oxygenator w Integrated AF w Hardshell Res. 3CX*FX15RE40CHeat-Exchanger, Cardiopulmonary Bypass46 reports
- Terumo® Advanced Perfusion System 1 195274Console, Heart-Lung Machine, Cardiopulmonary Bypass44 reports
- Capiox® RX Hollow Fiber Oxygenator with Hardshell Reservoir 3CX*RX25RWOxygenator, Cardiopulmonary Bypass39 reports