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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 17 of 17 Results
Related Medical Device Recalls
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Product Description
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Z-1636-2011 - Rubella IgG ELISA kit ; Rubella IgM ELISA kit BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human serum. 2 03/11/2011 BioCheck Inc
Z-1637-2011 - Toxoplasma IgG ELISA kit ; Toxoplasma IgM ELISA kit BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human serum. 2 03/11/2011 BioCheck Inc
Z-1638-2011 - CVM IgG ELISA kit ; CVM IgM ELISA kit BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human serum. 2 03/11/2011 BioCheck Inc
Z-1639-2011 - HSV-1 IgG ELISA kit ; HSV-1 IgM ELISA kit; BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human serum. 2 03/11/2011 BioCheck Inc
Z-1640-2011 - HSV-2 IgG ELISA kit ; HSV-2 IgM ELISA kit; BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human serum. 2 03/11/2011 BioCheck Inc
Z-1641-2011 - CK-MB ELISA kit ; BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human serum. 2 03/11/2011 BioCheck Inc
Z-1627-2011 - CEA ELISA Kit. BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human serum. 2 03/11/2011 BioCheck Inc
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