Medical Device Recalls
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1 to 5 of 5 Results
Recall Date to: 04/19/2014 PMA Number: P960040/S155 |
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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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Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following model... | 2 | 07/14/2009 | Boston Scientific CRM Corp |
Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, Models N118 and N11... | 2 | 08/18/2009 | Boston Scientific CRM Corp |
Boston Scientific TELIGEN, Implantable Cardiac Defibrillator, Models E102 and E110. Sterilized usin... | 2 | 08/18/2009 | Boston Scientific CRM Corp |
Boston Scientific TELIGEN, Implantable Cardiac Defibrillator, Models E102 and E110. Sterilized using... | 2 | 05/08/2010 | Boston Scientific CRM Corp |
Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models... | 2 | 10/17/2013 | Boston Scientific CRM Corp |
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