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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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GUIDANT VITALITY® DS VR Model T135 VR; EL Model T127 DR; 2ICD Model T165 DR; 2ICD Model T175 VR; 2E...
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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 VENTAK PRIZM VR (model 1860) and VENTAK PRIZM DR (model 1861) Automatic Implantable Cardiove...
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2
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09/28/2006
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Boston Scientific CRM Corp
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Guidant VITALITY 2 (models T165, T175), VITALITY DS (model T125), VITALITY EL (model T135), Implant...
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2
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07/27/2006
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Boston Scientific CRM Corp
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Guidant VITALITY 2 DR/VR (Models T165, T175) and Guidant VITALITY 2 EL DR/VR (Models T167, T177). I...
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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 VITALITY DS DR/VR (Models T125, T135), Guidant VITALITY EL (Model T127), Guidant VITALITY DR...
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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 VITALITY HE Implantable Cardioverter Defibrillator (model T180). Sterile EO. Guidant Corpo...
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2
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05/02/2006
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Guidant Corporation
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Guidant, Vitality HE ICD, Model: T180DDR, Sterile Lot, Guidant Corporation, Cardiac Rhythm Managemen...
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2
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10/07/2010
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Boston Scientific CRM Corp
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PRIZM 2 DR, model 1861 Automatic Implantable Cardioverter Defibrillator. Contents have been Sterili...
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2
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08/03/2005
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Guidant Corporation
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RESONATE EL ICD DR, Model D433, Sterile.
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2
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11/08/2017
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Boston Scientific Corporation
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RESONATE EL ICD VR, Model D432, Sterile.
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2
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11/08/2017
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Boston Scientific Corporation
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