Medical Device Recalls
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31 to 32 of 32 Results
Recall Date to: 09/01/2015 PMA Number: P010012 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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VITALITY DR HE Implantable Cardioverter Defibrillator (model T180). Sterile EO. Guidant Corporation... | 2 | 07/11/2007 | Boston Scientific CRM Corp |
Guidant CONTAK RENEWAL 3 (models H170, H175) CONTAK RENEWAL 3 HE (models H177, H179) Cardiac Resynch... | 2 | 07/27/2006 | Boston Scientific CRM Corp |
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