Terumo Cardiovascular Systems Corporation
6200 Jackson Road, ANN ARBOR, MI, US
Registered product codes
14 product codes
Recent MDR events
7,822 on file
- Virtuosaph Plus with Radial IndicationJul 31, 2026Injury1124841-2026-00076
- Advanced Perfusion System 1Jul 30, 2026Malfunction1828100-2026-00204
- Advanced Perfusion System 1Jul 30, 2026Malfunction1828100-2026-00205
- Advance Perfusion System 1Jul 29, 2026Malfunction1828100-2026-00202
- Advanced Perfusion System 1Jul 29, 2026Malfunction1828100-2026-00203
- Virtuosaph Plus with Radial IndicationJul 28, 2026Malfunction50053490
- Capiox FX Advance Hollow Fiber Oxygenator w Integrated AF w Hardshell Res.Jul 28, 2026Injury1124841-2026-00075
- CAPIOX® FX ADVANCE HOLLOW FIBER OXYGENATOR W INTEGRATED AF W HARDSHELL RES.Jul 22, 2026Malfunction1124841-2026-00074
- ADVANCED PERFUSION SYSTEM 1Jul 21, 2026Malfunction1828100-2026-00198
- ADVANCED PERFUSION SYSTEM 1Jul 21, 2026Malfunction1828100-2026-00199
Recalls
358 on file
- Open, ClassifiedJun 24, 2025
Due to an error in assembly of the thermistor within some units, the affected probes will experience inaccuracy in measured shunt sensor temperature. Additionally, following changes in patient temperature without an in vivo recalibration, affected probes may experience inaccuracy in other measured parameters, including pCO2, pO2, pH, Potassium and calculated parameters, including BE, Bicarbonate, Arterial Oxygen Saturation, Delivered Oxygen, Area Under of the Curve of Delivered Oxygen, Oxygen Consumption, and Oxygen Extraction Ratio, which utilize temperature as an input. Inaccurate data may lead to inappropriate user response.
View FDA record ↗ - Open, ClassifiedMar 31, 2025
During some clinical cases, it has been observed that the SO2 value may periodically appear as dashes on the Touchscreen Display indicating unavailable data. In these cases, a yellow low-limit alarm will also be triggered to the user, due to the dashed-out value.
View FDA record ↗ - Open, ClassifiedMar 29, 2024
Pressure relief valve included in certain lots of cardiovascular procedure kits was reportedly opening at approximately 200-300mmHg versus 400mmHg, potential myocardial tissue damage potentially requiring surgical or medical/pharmacological intervention
View FDA record ↗ - Open, ClassifiedApr 5, 2023
Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor component that is improperly bonded to the oxygenator port. This may result in a leak at the point where the arterial thermistor is improperly bonded to the oxygenator port.
View FDA record ↗ - Open, ClassifiedApr 5, 2023
Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor component that is improperly bonded to the oxygenator port. This may result in a leak at the point where the arterial thermistor is improperly bonded to the oxygenator port.
View FDA record ↗ - Open, ClassifiedApr 5, 2023
Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor component that is improperly bonded to the oxygenator port. This may result in a leak at the point where the arterial thermistor is improperly bonded to the oxygenator port.
View FDA record ↗ - TerminatedApr 18, 2018
Update to cooler-heater cleaning instructions.
View FDA record ↗ - TerminatedApr 18, 2018
Update to cooler-heater cleaning instructions.
View FDA record ↗ - TerminatedApr 18, 2018
Update to cooler-heater cleaning instructions.
View FDA record ↗ - TerminatedMar 14, 2017
Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and Level Sensor Gel Pads due to non-compliant labeling because the product expiration date is displayed in a format that may not be recognizable to all users.
View FDA record ↗
Compliance history
Matched by FEI 1828100.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.