Medical Device Recalls
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1 result found
Recall Number: Z-1237-2019 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DELFIA¿ hCG Kit, In Vitro Diagnostic for the determination of human gonadotropin (hCG) Product Code... | 2 | 04/27/2019 |
FEI # 3002808498 PerkinElmer Life and Analytical Sciences, Wallac, OY |
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