Medical Device Recalls
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1 result found
510(K) Number: K033300 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Vitros Myoglobin Calibrators, Product Code 6801043 For use in the calibration of the VITROS ECi/ECiQ... | 2 | 02/15/2019 |
FEI # 2250051 Ortho Clinical Diagnostics Inc |
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