Medical Device Recalls
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1 result found
510(K) Number: K182940 |
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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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| Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only | 2 | 12/11/2025 |
FEI # 1000132332 Nipro Medical Corporation |
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