Medical Device Recalls
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41 to 45 of 45 Results
PMA Number: P030054 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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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 ATLAS + HF Tiered-therapy cardioverter/defibrillator with bi... | 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 |
Implantable Cardioverter-Defibrillator Models affected include the following: Atlas+ Models V-... | 2 | 04/13/2005 | St Jude Medical |
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