Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K100433 |
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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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IMMULITE 2000/IMMULITE 2000XPi Systems CMM CMV IgM Assay, REF/Catalog Number L2KCM2(D) - 200 tests (... | 2 | 10/27/2016 | Siemens Healthcare Diagnostics, Inc. |
IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay, REF/Catalog Number LKCM1(D) - 100 tests (US), Sie... | 2 | 10/27/2016 | Siemens Healthcare Diagnostics, Inc. |
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