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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K183088
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FDA Recall
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Atellica IM Erythropoietin (EPO) Assay (100 Test) 2 03/11/2024 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
ADVIA Centaur Erythropoietin (EPO) Assay (100 Test) 2 03/11/2024 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
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