Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Z-1700-2016 - 1) VITROS® Immunodiagnostic Products Total Beta-hCG II Reagent Pack (Unique Device Identifier No. 10758750002320, 20758750002327) and the 2)VITROS® Immunodiagnostic Products Total Beta-hCG II Calibra... | 2 | 05/20/2016 |
FEI # 1000136573 Ortho-Clinical Diagnostics |
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