Every recall we track for St. Jude Medical — 13 in all — plus the complaints and injury reports the public filed about them.
St. Jude Medical recalls CardioMEMS Heart Failure System models CM3100 and CM4000 due to patient data duplication or missing information during cloud migration. Affected units have specific serial numbers.
St. Jude Medical recalls Merlin.net Patient Care Network Heart Failure Web Application (Model MN6000) due to data migration issues preventing transmission of heart failure readings.
St. Jude Medical recalls Agilis NxT Steerable Introduer model REF 408309 with short dilators that may not extend outside the sheath, posing a risk of injury during medical procedures.
St. Jude Medical recalls CardioMEMS HF System Patient Electronics (PES) Model CM1100 due to potential interference with medical devices like pacemakers and glucose monitors during readings.
St. Jude Medical recalls CardioMEMS HF System Patient Electronics (PES) Model CM1000 due to potential radiofrequency interference with medical devices like pacemakers and glucose monitors during readings. Affected units have specific serial numbers listed in the recall.
St. Jude Medical recalls CardioMEMS HF System Patient Electronics (PES) Model CM1010 due to potential radiofrequency emissions interfering with implantable medical devices like pacemakers and defibrillators.
St. Jude Medical recalls CardioMEMS HF System Hospital Electronics (HES) Model CM3000 due to potential radiofrequency emissions interfering with pacemakers, defibrillators, and other medical devices during use.
St. Jude Medical recalls CardioMEMS HF System PA Sensors (Model CM2000) that may operate outside intended frequency range at elevations over 2,000 ft, causing inaccurate readings. Affected units have specific UDI/DI codes listed in the recall.
St. Jude Medical recalls CardioMEMS HF System PA Sensor and Delivery System Model CM2000 for potential inaccurate readings at elevations over 2,000 ft. due to radiofrequency operation outside intended range. This may affect heart failure patients using the device.
St. Jude Medical recalls CardioMEMS HF System PA Sensors (Model CM2000) that may give inaccurate readings above 2,000 ft elevation due to radiofrequency issues. This could affect heart failure monitoring accuracy.
