Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K081008 |
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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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Single Analyte DAU Calibrator (5 mL) Norbuprenorphine: Cutoff Calibrator; IVD - for in vitro diagn... | 3 | 03/21/2014 | Lin-Zhi International Inc |
Single Analyte Urine DAU Control (5 m L Norbuprenorphine, Level II control For In Vitro Diagnostic... | 3 | 11/25/2013 | Lin-Zhi International Inc |
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