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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 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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Guidant CONTAK RENEWAL 3 (models H170, H175) CONTAK RENEWAL 3 HE (models H177, H179) Cardiac Resynch...
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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 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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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 (model H170, H175) CONTAK RENEWAL 3 HE (model H177, H179) Cardiac Resynchronization...
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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 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 DR HE Implantable Cardioverter Defibrillator (model T180). Sterile EO. Guidant Corporation...
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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 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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