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Terumo Cardiovascular Systems Recalls
223 recalls on record · June 27, 2012 to July 2, 2025 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 2, 2025Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe, Cat. No. CDI753TK - CDI OneView BPM Probe Tri
Hazard: 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.
April 9, 2025Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Catalog Number REF CD1754
Hazard: 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.
April 10, 2024Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Cardiovascular Procedure Kits that include High Crack Check Valve PN 205307A Part Number: 6375 16010 62974 65246 6
Hazard: 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
April 12, 2023Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls CAPIOX FX25 Hollow Fiber Oxygenator, Catalog Numbers 3CX*FX25REC, 3CX*FX25RWC
Hazard: 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.
April 12, 2023Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls CAPIOX NX19 Hollow Fiber Oxygenator, Catalog Number 3CX*NX19RE
Hazard: 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.
April 12, 2023Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls CAPIOX RX15 Hollow Fiber Oxygenator, Catalog Number 3CX*RX15RE30
Hazard: 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.
April 27, 2022Medical DevicesFDA
Terumo Cardiovascular Systems Corp recalls Cardiovascular Procedure Kit catalog # 76645 & 73806
Hazard: Potential for Cardiovascular Procedure Kit packaging damage that occurred during shipping.
September 1, 2021Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion System 1 Electronic Patient Gas System Catalog #: 801188
Hazard: intermittent failure causes a blender initialization fault upon start-up, or during an EPGS calibration attempt following the 15-minute warm-up period. The control sliders on the Central Control Monitor (CCM) are disabled and the gas system can only be controlled by the local control knobs
June 9, 2021Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls The Sarns TCM II (system) is a source of temperature-controlled water for blood heat exchangers used in an extracorporea
Hazard: Terumo CVS has been unable to validate a cleaning protocol to satisfy current regulatory concerns and expectations. As a result, an updated cleaning protocol will not be developed by Terumo CVS and it has been determined that the best course of action is for users to discontinue use of and dispose of HX2, TCM I and TCM II devices.
June 9, 2021Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls The Sarns Temperature Control and Monitor unit (TCM) is a source of temperature-controlled water for blood heat exchange
Hazard: Terumo CVS has been unable to validate a cleaning protocol to satisfy current regulatory concerns and expectations. As a result, an updated cleaning protocol will not be developed by Terumo CVS and it has been determined that the best course of action is for users to discontinue use of and dispose of HX2, TCM I and TCM II devices.
June 9, 2021Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls The Terumo HX2 Temperature Management System provides temperature control of two independent water circuits that directl
Hazard: Terumo CVS has been unable to validate a cleaning protocol to satisfy current regulatory concerns and expectations. As a result, an updated cleaning protocol will not be developed by Terumo CVS and it has been determined that the best course of action is for users to discontinue use of and dispose of HX2, TCM I and TCM II devices.
April 14, 2021Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Consist of a distal connection mechanism (either standard Terumo Ball Quick Connect or Terumo Shaft Quick Connect), an a
Hazard: There is a potential for the stainless steel locking plates on the device's sternal retractor locking mechanism to fracture.
December 23, 2020Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls (1) Capiox FX25 (West) Advance Oxygenator- with left port, 4-liter Reservoir, XC modified to Advance, Sterile Catalog
Hazard: Capiox FX25 Advance oxygenator may be the incorrect configuration (East vs. West)
September 23, 2020Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x3/32, Catalog Number 5791 - Product Usage: intended for use
Hazard: Internal testing at the supplier, revealed that a crimped wire was placed into an air bubble detector (ABD) sensor connector backwards, preventing the crimped wire from locking into the mating wire connector. This intermittent connection may result in false air bubble alarms.
September 23, 2020Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x1/16 UAS BLK, Catalog Number 5785 - Product Usage: intended
Hazard: Internal testing at the supplier, revealed that a crimped wire was placed into an air bubble detector (ABD) sensor connector backwards, preventing the crimped wire from locking into the mating wire connector. This intermittent connection may result in false air bubble alarms.
September 23, 2020Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 3/8x3/32, Catalog Number 5773 - Product Usage: intended for use
Hazard: Internal testing at the supplier, revealed that a crimped wire was placed into an air bubble detector (ABD) sensor connector backwards, preventing the crimped wire from locking into the mating wire connector. This intermittent connection may result in false air bubble alarms.
February 19, 2020Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion Assembly Pump Guts, 4 Inch, Catalog Number 801805 - Product Usage: is indicated for use for up
Hazard: These roller pumps were assembled with pump shafts that may fail at the location of the thread where a locknut is installed. The failure is associated with a noise that is atypical of roller pump operation. The noise is caused when an unsecured shaft end contacts the rotating pulley of the roller pump. Prolonged use of a roller pump in this condition could lead to an eventual pump stop, resulting in the inability to create pump flow due to pulley loosening and drive belt damage.
February 19, 2020Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion Assembly Pump Guts, 6 Inch, Catalog Number 801798 - is indicated for use for up to 6 hours in
Hazard: These roller pumps were assembled with pump shafts that may fail at the location of the thread where a locknut is installed. The failure is associated with a noise that is atypical of roller pump operation. The noise is caused when an unsecured shaft end contacts the rotating pulley of the roller pump. Prolonged use of a roller pump in this condition could lead to an eventual pump stop, resulting in the inability to create pump flow due to pulley loosening and drive belt damage.
February 19, 2020Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion System 1 Roller Pump, 6 Inch, Catalog Number 816571 - Product Usage: is indicated for use for
Hazard: These roller pumps were assembled with pump shafts that may fail at the location of the thread where a locknut is installed. The failure is associated with a noise that is atypical of roller pump operation. The noise is caused when an unsecured shaft end contacts the rotating pulley of the roller pump. Prolonged use of a roller pump in this condition could lead to an eventual pump stop, resulting in the inability to create pump flow due to pulley loosening and drive belt damage.
February 19, 2020Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion System 1 Roller Pump, 4 Inch, Catalog Number 816570 - Product Usage: is indicated for use for
Hazard: These roller pumps were assembled with pump shafts that may fail at the location of the thread where a locknut is installed. The failure is associated with a noise that is atypical of roller pump operation. The noise is caused when an unsecured shaft end contacts the rotating pulley of the roller pump. Prolonged use of a roller pump in this condition could lead to an eventual pump stop, resulting in the inability to create pump flow due to pulley loosening and drive belt damage.
August 7, 2019Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Capiox NX19 Oxygenator (West Orientation P/N:CXOT281 Exported only to Japan for inclusion into convenience kits
Hazard: Capiox NX19 Oxygenator may contain a non-functioning arterial thermistor component
August 7, 2019Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Capiox NX19 Oxygenator (East Orientation), P/N: CXOT280 Exported only to Japan for inclusion into convenience ki
Hazard: Capiox NX19 Oxygenator may contain a non-functioning arterial thermistor component
August 7, 2019Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Capiox NX19 Oxygenator With Reservoir (West Orientation) P/N: 3CX*NX19RW
Hazard: Capiox NX19 Oxygenator may contain a non-functioning arterial thermistor component
August 7, 2019Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Capiox NX19 Oxygenator With Reservoir (East Orientation) P/N: 3CX*NX19RE
Hazard: Capiox NX19 Oxygenator may contain a non-functioning arterial thermistor component
June 19, 2019Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas Blender, Catalog #: 801188, UDI
Hazard: An intermittent failure which causes a blender initialization fault upon start-up or during an EPGS calibration attempt leads to the Central Control Monitor control sliders being disabled, such that the gas system can only be controlled by the local control knobs.
May 22, 2019Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion System 1 Electronic Patient Gas System, Catalog # 801188, UDI 00886799000588 The electronic
Hazard: The gas flow rate output of the EPGS may be inaccurate due to a defect in the internal flowmeter.
March 6, 2019Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Cardiovascular Procedure Kit (CLR MP4 COIL 2 SPIKE) Catalog Number: 140222
Hazard: Presence of natural rubber latex is not declared in the label
October 31, 2018Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls VirtuoSaph Plus Endoscopic Vessel Harvesting System, Catalog Number: VSP550EX Product Usage: The VittuoSaph¿ Plus En
Hazard: The system's IFU contains a list of generators that the have been deemed compatible. Recent reports indicate that one energy platform is not compatible with the system. Therefore, it has been removed from the list of compatible generators within the IFU.
October 24, 2018Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System, Catalog#: 801188
Hazard: The service manual was not updated at the time of the release of software version 1.30.
October 3, 2018Medical DevicesFDA
Terumo Cardiovascular Systems Corporation recalls Terumo 220/240V AC, Advanced Perfusion System Platform (APS) for use in cardiopulmonary bypass procedures. Catalog Nu
Hazard: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the base unit circuit board) were not torqued to specification. It is possible that a screw which has not been properly torqued can go undetected during manufacturing testing and may loosen over time, resulting in the potential for an electrical short in the system