Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-1078-2017 - Sekisui Diagnostics Ammonia L3K® Assay; Catalog Number: 293-80-91 and 293-10 For the IN VITRO quantitative measurement of ammonia concentration in plasma | 2 | 01/23/2017 | Sekisui Diagnostics P.E.I. Inc. |
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