Medical Device Recalls
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1 result found
510(K) Number: K130528 |
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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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| BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack | 2 | 05/10/2023 | Bio-Rad Laboratories, Inc. |
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