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FDA Warns About Heart Defibrillators After Two People Die
St. Jude Medical 1207–36 defibrillator— – PMCT slices through the... | Download Scientific Diagram
PDF) Characteristics of patients and implantable defibrillators associated with failure to sense device alert systems
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ICD and CRT-D Battery Advisory | Abbott
Battery performance alert update on Class I recall of St. Jude Medical's ICDs and CRT-Ds
Recurrent implantable cardioverter-defibrillator shocks due to automatic deactivation of a right ventricular lead noise discrimi
Troubleshooting Implanted Cardioverter Defibrillator Sensing Problems I | Circulation: Arrhythmia and Electrophysiology
After 2 deaths, patients warned about heart defibrillators | CNN
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Defective St. Jude ICD / CRT-D Devices - Long Island Accident Attorneys | RGLZ Personal Injury Law
St. Jude Medical Played Down Defibrillator Failures for Years, F.D.A. Says - The New York Times
St. Jude Medical Expands Portfolio of MRI-Compatible Devices to High Voltage in Europe | DAIC
JCM | Free Full-Text | High Incidence of Inappropriate Alarms in Patients with Wearable Cardioverter-Defibrillators: Findings from the Swiss WCD Registry
2 deaths lead to recall of St. Jude heart devices | CBC News
April 2013 – The World of Implantable Devices
After 2 deaths, patients warned about heart defibrillators | CNN
St. Jude Medical Defibrillators - Devices at Risk, Recalls
Saint Jude Medical Discrimination | Cardiocases
After 2 deaths, patients warned about heart defibrillators | CNN
FDA Warns About Heart Defibrillators After Two People Die
Recurrent implantable cardioverter-defibrillator shocks due to automatic deactivation of a right ventricular lead noise discrimi
St. Jude Medical Defibrillators - Devices at Risk, Recalls