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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K012077
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FDA Recall
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SIEMENS IMMULITE/IMMULITE 2000 Systems Rubella IgM (RUM), REF/Catalog Number for US: L2KRM2(D), Siem... 2 10/13/2016 Siemens Healthcare Diagnostics, Inc.
SIEMENS IMMULITE/IMMULITE 1000 Systems Rubella IgM (RUM), REF/Catalog Number LKRM1 (OUS), Siemens Ma... 2 10/13/2016 Siemens Healthcare Diagnostics, Inc.
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