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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-3103-2024
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ADVIA Centaur CA 19-9 (50 Test)-In vitro diagnostic use in the quantitative measurement of the CA 19... 2 09/11/2024 FEI # 1219913
Siemens Healthcare Diagnostics, Inc.
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