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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K003291
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FDA Recall
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Atellica IM aTPO Assay, Material Number 10995466 (100 Test) and 10995467 (500 Test) 2 09/27/2024 Siemens Healthcare Diagnostics, Inc.
ADVIA Centaur aTPO Assay, Material Number 10630886 (100 Test) and 10630887 (500 Test) 2 09/27/2024 Siemens Healthcare Diagnostics, Inc.
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