Medical Device Recalls
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1 result found
510(K) Number: K883696 |
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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 Flo-Rester, Disposable internal vessel occluder, distributed in the following sizes: a) Prod... | 2 | 01/05/2024 | Baxter Healthcare Corporation |
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