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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Z-1237-2019 - DELFIA® hCG Kit, In Vitro Diagnostic for the determination of human gonadotropin (hCG) Product Code: A007-101 - Product Usage: Quantitative determination of human gonadotrophin (hCG) in serum. 2 04/27/2019 FEI # 3002808498
PerkinElmer Life and Analytical Sciences, Wallac, OY
Z-1239-2019 - AutoDELFIA® hCG Kit, In Vitro Diagnostic for the determination of human gonadotropin (hCG) Product Code: B007-112 - Product Usage: Quantitative determination of human gonadotrophin (hCG). 2 04/27/2019 FEI # 3002808498
PerkinElmer Life and Analytical Sciences, Wallac, OY
Z-1238-2019 - AutoDELFIA® hCG Kit, In Vitro Diagnostic for the determination of human gonadotropin (hCG) Product Code: B007-101 - Product Usage: Quantitative determination of human gonadotrophin (hCG). 2 04/27/2019 FEI # 3002808498
PerkinElmer Life and Analytical Sciences, Wallac, OY
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