Medical Device Recalls
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1 result found
510(K) Number: K232467 |
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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 AK 98 Dialysis Machine, Hemodialysis Delivery System, Product Code 955607. As of February 20... | 1 | 11/13/2024 |
FEI # 1417572 Baxter Healthcare Corporation |
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