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VITROS Chemistry Products LAC Slides. Catalog Number: 8150112. 1 Sales Unit = contains 5 cartridges of 18 slides, for a total of 90 tests.

FDA Recall
Open, Classified ·Ortho-Clinical Diagnostics, Inc.·Product code KHP·July 29, 2025

Atellica IM Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 11206250 All lots

FDA Recall
Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022

Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995561 All lots

FDA Recall
Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022

VIDAS CLINICAL VIDAS ESTRADIOL II 60 TESTS, CATALOG 30431-01

FDA Recall
Open, Classified ·Biomerieux Inc·Product code CHP·November 9, 2022

VIDAS Estradiol II, REF 30431-01

FDA Recall
Open, Classified ·bioMerieux, Inc.·Product code CHP·September 22, 2021

Atellica IM Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995562 All lots

FDA Recall
Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022

ADVIA Centaur Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10490889 All lots

FDA Recall
Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022

ADVIA Centaur Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10491445 All lots

FDA Recall
Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022

ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative detection of estradiol SMN: 10697757 All lots

FDA Recall
Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code CHP·March 3, 2022

Chemistry Products LAC Slides. Catalog Number: 8433880. 1 Sales Unit = contains 5 cartridges of 60 slides, for a total of 300 tests.

FDA Recall
Open, Classified ·Ortho-Clinical Diagnostics, Inc.·Product code KHP·July 29, 2025