Medical Device Recalls
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1 result found
510(K) Number: K982426 |
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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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SPIFE Alkaline Hemoglobin Kit, Cat. No. 3415, for use in the separation and quantitation of hemo... | 3 | 11/05/2019 | Helena Laboratories, Corp. |
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