Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Z-0542-2020 - myCordella Patient Kit without ECG, The Cordella System is a comprehensive at-home heart failure management platform that provides the clinician tools to monitor the progression of heart failure. | 2 | 11/22/2019 |
FEI # 3013900541 ENDOTRONIX |
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