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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 32 Results
Recall Date to: 07/02/2015 PMA Number: P030054
 
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Implantable Cardioverter-Defibrillator Models affected include the following: Atlas+ Models V-... 2 04/13/2005 St Jude Medical
Implantable Cardioverter Defibrilators Epic DR/HF (V-233/V-337/V-338), Epic Plus DR/VR/HF (V-236/... 2 07/19/2005 St Jude Medical
Implantable Cardioverter Defibrillator EPIC HF Tiered-therapy cardioverter/defibrillator with biven... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator EPIC HF Tiered-Therapy Cardioverter/Defibrillator with Biven... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator EPIC HF Tiered-therapy Cardioverter/defibrillator with biven... 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 DR Tiered-therapy cardioverter/defibrillator, Model V-2... 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 + DR Tiered-therapy cardioverter/defibrillator, Model V... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator EPIC + HF Tiered-therapy cardioverter/defibrillator with biv... 2 08/19/2008 St Jude Medical CRMD
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