Medical Device Recalls
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31 to 35 of 35 Results
Recall Date to: 11/23/2014 PMA Number: P910023 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Implantable Cardioverter Defibrillator ATLAS II+ DR Tiered-therapy cardioverter/defibrillator, Mod... | 2 | 08/19/2008 | St Jude Medical CRMD |
Implantable Cardioverter Defibrillator ATLAS 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 ATLAS II+ HF Tiered-therapy cardioverter/defibrillator with ... | 2 | 08/19/2008 | St Jude Medical CRMD |
Ellipse Implantable Cardioverter Defibrillators (ICDs), Model No. CD1275, CD1311, CD2275, CD2311, C... | 2 | 09/03/2014 | St Jude Medical Cardiac Rhythm Management Division |
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