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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-1513-2013
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ADVIA Centaur® iPTH ReadyPack Assay 500 Tests; REF 10492369, 10493615, 1049361. For in vitro diag... 2 06/06/2013 FEI # 1219913
Siemens Healthcare Diagnostics, Inc
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