Medical Device Recalls
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31 to 36 of 36 Results
PMA Number: P010012 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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CONTAK RENEWAL 3 RF (model H210, H215), CONTAK RENEWAL 3 RF HE (model H217, H219) cardiac resynchron... | 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 |
The PRM is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with B... | 2 | 09/02/2022 | Boston Scientific Corporation |
VIGILANT X4 CRT-D, Model G247, Sterile. Cardiac Resynchronization Therapy Defibrillators (CRT-D... | 2 | 11/08/2017 | Boston Scientific Corporation |
MOMENTUM X4 CRT-D, Model G138, Sterile. | 2 | 11/08/2017 | Boston Scientific Corporation |
RESONATE X4 CRT-D, Model G447, Sterile. | 2 | 11/08/2017 | Boston Scientific Corporation |
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