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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 34 Results
Recall Date to: 04/21/2014 PMA Number: P910023
 
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Atlas DR, Models V-240 2 11/16/2005 St Jude Medical
Atlas VR, Models V-199 2 11/16/2005 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 ATLAS + DR Tiered-therapy cardioverter/defibrillator, Model ... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator ATLAS + HF Tiered-therapy cardioverter/defibrillator with bi... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator ATLAS + HF Tiered-therapy cardioverter/defibrillator with bi... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator ATLAS + HF Tiered-therapy cardioverter/defibrillator with bi... 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
Implantable Cardioverter Defibrillator ATLAS DR Tiered-therapy cardioverter/defibrillator, Model V-... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter Defibrillator ATLAS II DR Tiered-therapy cardioverter/defibrillator, Model... 2 08/19/2008 St Jude Medical CRMD
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