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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 32 Results
Recall Date to: 10/21/2014 PMA Number: P030054
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Product Description
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Recall
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FDA Recall
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Implantable Cardioverter Defibrillator EPIC II VR Tiered-therapy cardioverter/defibrillator, Model... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator EPIC II DR Tiered-therapy cardioverter/defibrillator, Model... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator EPIC II+ DR Tiered-therapy cardioverter/defibrillator, Mode... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator EPIC DR Tiered-Therapy Cardioverter/Defibrillator, Model V-... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator EPIC VR Tiered-therapy Cardioverter/Defibrillator, Model V-... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator EPIC II HF Tiered-therapy cardioverter/defibrillator with B... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator ATLAS II+ HF Tiered-therapy cardioverter/defibrillator with ... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator EPIC II+ HF Tiered-therapy cardioverter/defibrillator with ... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator EPIC II+ HF Tiered-therapy cardioverter/defibrillator with ... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator ATLAS + VR Tiered-therapy cardioverter/defibrillator, Model ... 2 08/19/2008 St Jude Medical CRMD
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