Medical Device Recalls
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1 result found
510(K) Number: K160735 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled as the following kits: ... | 2 | 04/23/2019 | Fenwal Inc |
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