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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Z-1020-2022 - Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995561 All lots 2 04/29/2022 Siemens Healthcare Diagnostics, Inc.
Z-1021-2022 - Atellica IM Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995562 All lots 2 04/29/2022 Siemens Healthcare Diagnostics, Inc.
Z-1025-2022 - ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative detection of estradiol SMN: 10697757 All lots 2 04/29/2022 Siemens Healthcare Diagnostics, Inc.
Z-1023-2022 - ADVIA Centaur Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10490889 All lots 2 04/29/2022 Siemens Healthcare Diagnostics, Inc.
Z-1024-2022 - ADVIA Centaur Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10491445 All lots 2 04/29/2022 Siemens Healthcare Diagnostics, Inc.
Z-1022-2022 - Atellica IM Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 11206250 All lots 2 04/29/2022 Siemens Healthcare Diagnostics, Inc.
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