Medical Device Recalls
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1 result found
510(K) Number: K052883 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b... | 2 | 09/28/2023 |
FEI # 1417572 Baxter Healthcare Corporation |
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