Medical Device Recalls
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31 to 32 of 32 Results
Recall Date to: 07/28/2015 PMA Number: P010012 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Guidant, CONTAK RENEWAL 3/3RF Models H170, H175, H177, H179, H210, H215, H217, H219, Guidant Corpor... | 2 | 10/07/2010 | Boston Scientific CRM Corp |
Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N118, N119. ... | 2 | 10/18/2014 | Boston Scientific CRM Corp |
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