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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0620-2019 - ultra2 Genesys Variants Analyzer, REF 03-01-0045 intended to be used with automated high performance liquid chromatography (HPLC) systems employing ion exchange chromatography. For in vitro diagnostic... 2 12/18/2018 Clark Laboratories, Inc. (dba,Trinity Biotech USA)
Z-0621-2019 - Genesys Analytical Column, REF 01-05-0017 intended to be used with automated high performance liquid chromatography (HPLC) systems employing ion exchange chromatography. For in vitro diagnostic use on... 2 12/18/2018 Clark Laboratories, Inc. (dba,Trinity Biotech USA)
Z-0624-2019 - Genesys Diluent Reagent, REF 01-03-0019 intended to be used with automated high performance liquid chromatography (HPLC) systems employing ion exchange chromatography. For in vitro diagnostic use only... 2 12/18/2018 Clark Laboratories, Inc. (dba,Trinity Biotech USA)
Z-0623-2019 - Genesys 2 Reagent, REF 01-03-0022 intended to be used with automated high performance liquid chromatography (HPLC) systems employing ion exchange chromatography. For in vitro diagnostic use only. 2 12/18/2018 Clark Laboratories, Inc. (dba,Trinity Biotech USA)
Z-0622-2019 - Genesys 1 Reagent, REF 01-03-0020 intended to be used with automated high performance liquid chromatography (HPLC) systems employing ion exchange chromatography. For in vitro diagnostic use only. 2 12/18/2018 Clark Laboratories, Inc. (dba,Trinity Biotech USA)
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