Medical Device Recalls
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1 result found
510(K) Number: K030067 |
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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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| VITROS Immunodiagnostic Products HBsAg Controls, Product Code 6800598 For in vitro diagnostic use... | 3 | 10/25/2016 |
FEI # 1000136573 Ortho-Clinical Diagnostics |
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