Medical Device Recalls
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1 result found
510(K) Number: K931756 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determin... | 3 | 07/15/2022 | R & D Systems, Inc. |
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