Medical Device Recalls
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31 to 37 of 37 Results
Recall Date to: 12/01/2015 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 + 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 + DR Tiered-therapy cardioverter/defibrillator, Model ... | 2 | 08/19/2008 | St Jude Medical CRMD |
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 |
Ellipse Implantable Cardioverter Defibrillators (ICDs), Model No. CD1275, CD1311, CD2275, CD2311, C... | 2 | 09/03/2014 | St Jude Medical Cardiac Rhythm Management Division |
Atlas VR, Models V-199 | 2 | 11/16/2005 | St Jude Medical |
Atlas DR, Models V-240 | 2 | 11/16/2005 | St Jude Medical |
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