Medical Device Recalls
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1 result found
510(K) Number: K191658 |
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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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| CARESAFE utilized in gravity IV administration sets and pump administration sets utilized with BBMI'... | 2 | 11/26/2025 | B Braun Medical Inc |
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