Medical Device Recalls
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510(K) Number: K081938 |
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Product Description
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Recall
Class |
FDA Recall
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Recalling Firm
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Sekisui Diagnostics Sekure Chemistry Acetaminophen L3K , Ref. 506-30. The firm names on the label a... | 2 | 09/12/2017 | Beckman Coulter Inc. |
Sekure Chemistry Sekisui Diagnostics Acetaminophen L3K Assay, In-vitro Diagnostic Catalog Number: ... | 2 | 03/14/2016 | Sekisui Diagnostics P.E.I. Inc. |
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