Medical Device Recalls
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1 result found
Recall Number: Z-0164-2016 |
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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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| Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement; List Number: ... | 2 | 10/26/2015 |
FEI # 3000303338 Sentinel CH SpA |
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