Every recall we track for St. Jude Medical, Cardiac Rhythm Management Division — 10 in all — plus the complaints and injury reports the public filed about them.
St. Jude Medical recalls Merlin.net MN5000 software v11.7 due to potential device programming risks. Affected users should contact for updates.
St. Jude Medical recalls Merlin PCS 365:3650 programmer software version 3330 v26.0.1 rev 1 or earlier for potential overestimated battery life displays in pacemakers.
St. Jude Medical recalls Merlin 2 PCS MER37000 programmer software version 1.1.2 rev 1 or earlier due to potential device malfunction. Affected units have specific UDI/DI numbers.
St. Jude Medical recalls Gallant VR Implantable Cardioverter Defibrillators with Bluetooth malfunction that reduces remote monitoring and battery life. Affected units have specific serial numbers and expiration dates.
St. Jude Medical is a leading manufacturer of cardiac rhythm management products, including pacemakers, defibrillators, and other cardiac devices.
St. Jude Medical recalls Merlin 2 PCS MER3700 programmer software version v1.X.X (serial numbers listed) due to potential incorrect test execution during in-clinic procedures on implantable defibrillators.
St. Jude Medical recalls Gallant DR Implantable Cardioverter Defibrillators with REF # CDDRA500Q that may lose Bluetooth communication, reducing remote monitoring and battery life. Affected units were sold between 2018 and 2022.
St. Jude Medical recalls Gallant HF Implantable Cardioverter Defibrillators with specific serial numbers due to Bluetooth malfunction causing loss of remote monitoring and reduced battery life.
St Jude Medical recalls Ellipse cardioverter defibrillators with specific serial numbers that may lose wireless communication with doctors, preventing remote monitoring. Affected devices require immediate attention.
St Jude Medical recalls Merlin PCS Programmer software model 3330 used with Confirm Rx ICM Model DM3500. Devices may display a low battery indicator due to memory corruption. Affected units have specific serial numbers listed in the recall notice.
