Medical Device Recalls
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31 to 32 of 32 Results
Recall Date to: 09/01/2015 PMA Number: P010012 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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VITALITY 2 EL DR/VR (model T167, T177). contents have been sterilized with gaseous ethylene oxide. ... | 2 | 07/11/2007 | Boston Scientific CRM Corp |
VITALITY AVT (model A155). Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies.... | 2 | 07/11/2007 | Boston Scientific CRM Corp |
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