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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Z-2416-2018 - Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D153ATG Product Usage: The device indicated for use in ICD pati... 2 07/10/2018 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2417-2018 - Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154ATG Product Usage: The device indicated for use in ICD pati... 2 07/10/2018 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2421-2018 - Medtronic EnTrust Escudo D144DRG (OUS distribution) Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular defibrillatio... 2 07/10/2018 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2419-2018 - Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154VRC Product Usage: The implantable cardioverter defibrillat... 2 07/10/2018 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2420-2018 - Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular defibrillatio... 2 07/10/2018 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Z-2418-2018 - Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D153VRC Product Usage: The implantable cardioverter defibrillat... 2 07/10/2018 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
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