Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K012077 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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