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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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VITALITY AVT (model A155). Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies....
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2
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07/11/2007
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Boston Scientific CRM Corp
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VITALITY 2 EL DR/VR (model T167, T177). contents have been sterilized with gaseous ethylene oxide. ...
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2
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07/11/2007
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Boston Scientific CRM Corp
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VITALITY 2 (model T165, T175), VITALITY DS (model T125, T135), VITALITY EL (model T127), Implantable...
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2
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07/11/2007
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Boston Scientific CRM Corp
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Guidant, CONTAK RENEWAL 3/3RF Models H170, H175, H177, H179, H210, H215, H217, H219, Guidant Corpor...
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2
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10/07/2010
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Boston Scientific CRM Corp
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Guidant VITALITY VR/DR, Implantable Cardioverter Defibrillator, ICD, Models 1870 and 1871. Guidan...
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2
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11/24/2007
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Boston Scientific CRM Corp
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Guidant Contak® Renewal® 3 CRT-D Model H170; 3CRT-D, Model H175; 3HE CRT-D, Model H177; 3HE CRT-D, M...
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2
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07/17/2009
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Boston Scientific CRM Corp
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Guidant CONTAK RENEWAL 4 AVT (model M170). Cardiac Resynchronization Therapy Defibrillator (CRT-D)...
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2
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05/02/2006
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Guidant Corporation
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Guidant CONTAK RENEWAL 4 (models H190, H195) CONTAK RENEWAL; 4 HE (model H197). Cardiac Resynchroni...
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2
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05/02/2006
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Guidant Corporation
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Guidant CONTAK RENEWAL 3 RF (models H210, H215), CONTAK RENEWAL 3 RF HE (models H217, H219) ,CONTAK ...
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2
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12/16/2006
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Guidant Corporation
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Guidant CONTAK RENEWAL 3 AVT (models M150, M155), CONTAK RENEWAL 3 AVT HE (models M157, M159), CONTA...
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2
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07/04/2006
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Guidant Corporation
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