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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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CONTAK RENEWAL 3 RF (models H210, H215), CONTAK RENEWAL 3 RF HE (models H217, H219), CONTAK RENEWAL ...
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3
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05/16/2006
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Guidant Corporation
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CONTAK RENEWAL 3 RF (model H210, H215), CONTAK RENEWAL 3 RF HE (model H217, H219) cardiac resynchron...
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2
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07/11/2007
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Boston Scientific CRM Corp
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CONTAK RENEWAL 3 DS HE, model H177 CRT-D Cardiac Resynchronization Therapy Defibrillator. Content...
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2
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08/03/2005
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Guidant Corporation
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CONTAK RENEWAL 3 CRT-D (model no. H170, H175, H177, H179). Cardiac Resynchronization Therapy Defibr...
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3
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05/23/2006
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Guidant Corporation
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CONTAK RENEWAL 3 CRT-D (model no. H170, H173, H175) and CONTAK RENEWAL 3 HE CRT-D(model no. H177 and...
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2
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06/30/2005
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Guidant Corporation
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CONTAK RENEWAL 3 (model H170, H175) CONTAK RENEWAL 3 HE (model H177, H179) Cardiac Resynchronization...
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2
|
07/11/2007
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Boston Scientific CRM Corp
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CONTAK RENEWAL 3 (Models H170), Guidant CONTAK RENEWAL 3 HE (Models H177, H179). Cardiac Resynchroni...
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2
|
05/08/2010
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Boston Scientific CRM Corp
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CONTAK RENEWAL (model H135) Heart Failure Device Cardiac Resynchronization Therapy Defibrillators (C...
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1
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06/30/2005
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Guidant Corporation
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Boston Scientific TELIGEN, Implantable Cardiac Defibrillator, Models E102 and E110. Sterilized usin...
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2
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08/18/2009
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Boston Scientific CRM Corp
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Boston Scientific LIVIAN Cardiac Resynchronization Therapy Defibrillator (CRT-D), models H220, H225,...
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2
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05/08/2010
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Boston Scientific CRM Corp
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