Medical Device Recalls
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1 result found
510(K) Number: K110726 |
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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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Roche Acetaminophen assay 03255379160-HAcetaminophen (P) 20767174160- cobas c Integra AAcetaminoph... | 2 | 04/25/2018 | Roche Diagnostics Corporation |
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