Medical Device Recalls
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31 to 32 of 32 Results
Recall Date to: 12/19/2014 PMA Number: P030054 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Implantable Cardioverter Defibrillator EPIC VR Tiered-therapy Cardioverter/Defibrillator, Model V-... | 2 | 08/19/2008 | St Jude Medical CRMD |
Implantable Cardioverter-Defibrillator Models affected include the following: Atlas+ Models V-... | 2 | 04/13/2005 | St Jude Medical |
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