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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K112343
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FDA Recall
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Centaur Syphilis Assay-SYP Kit, 200 Test - Product Usage: For in vitro diagnostic use in the qualita... 2 05/24/2021 Siemens Healthcare Diagnostics, Inc
Siemens ADVIA Centaur® Syphilis (SYPH) Assay , 200 ReadyPack Reference Number 10492493 Product... 2 08/20/2012 Siemens Healthcare Diagnostics, Inc