Medical Device Recalls
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1 to 3 of 3 Results
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-3037-2017 - EMBLEM S-ICD, Model A209, Subcutaneous Implantable Cardioverter Defibrillator, RX. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threate... | 2 | 08/16/2017 | Boston Scientific Corporation |
Z-3039-2017 - SQ-RX 1010 Pulse Generator, Rx. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do... | 2 | 08/16/2017 | Boston Scientific Corporation |
Z-3038-2017 - EMBLEM MRI S-ICD Model 219, Subcutaneous-Implantable Cardioverter Defibrillator, Rx. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-thr... | 2 | 08/16/2017 | Boston Scientific Corporation |
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