Medical Device Recalls
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1 result found
510(K) Number: K072908 |
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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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PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy | 2 | 06/24/2016 | Baxter Healthcare Corp. |
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