Medical Device Recalls
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1 result found
PMA Number: P960040/S012 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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VENTAK PRIZM Automatic Implantable Cardioverter Defibrillator (AICD). DR, model 1851, DR HE, model ... | 2 | 05/08/2010 | Boston Scientific CRM Corp |
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