Medical Device Recalls
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31 to 35 of 35 Results
PMA Number: P960040 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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VITALITY HE (model T180) Implantable Cardioverter Defibrillator (ICD). Sterile EO. Guidant Corporat... | 2 | 07/04/2006 | Guidant Corporation |
VITALITY DS (model T125) and VITALITY 2 (models T165, 175) ICD (implantable cardiac defibrillator) | 3 | 05/23/2006 | Guidant Corporation |
Guidant VITALITY HE Implantable Cardioverter Defibrillator (model T180). Sterile EO. Guidant Corpo... | 2 | 05/02/2006 | Guidant Corporation |
PRIZM 2 DR, model 1861 Automatic Implantable Cardioverter Defibrillator. Contents have been Sterili... | 2 | 08/03/2005 | Guidant Corporation |
Ventak PRIZM 2 DR, model 1861 Automatic Implantable Cardioverter Defibrillator (AICD), Dual Chamber,... | 1 | 06/30/2005 | Guidant Corporation |
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