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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 32 Results
Recall Date to: 04/25/2015 PMA Number: P010012
 
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Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N118, N119. ... 2 10/18/2014 Boston Scientific CRM Corp
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 LIVIAN Cardiac Resynchronization Therapy Defibrillator (CRT-D), models H220, H225,... 2 05/08/2010 Boston Scientific CRM Corp
Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, Models N118 and N11... 2 05/08/2010 Boston Scientific CRM Corp
CONTAK RENEWAL 3 (Models H170), Guidant CONTAK RENEWAL 3 HE (Models H177, H179). Cardiac Resynchroni... 2 05/08/2010 Boston Scientific CRM Corp
Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N118, N119. ... 2 01/13/2010 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 COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, Models N118 and N11... 2 08/18/2009 Boston Scientific CRM Corp
Guidant Contak® Renewal® 3 CRT-D Model H170; 3CRT-D, Model H175; 3HE CRT-D, Model H177; 3HE CRT-D, M... 2 07/17/2009 Boston Scientific CRM Corp
Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N118, N119. ... 2 07/14/2009 Boston Scientific CRM Corp
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