Medical Device Recalls
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1 result found
Recall Number: Z-0937-2014 |
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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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| Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized microcoagulation test intended to be ... | 2 | 02/06/2014 |
FEI # 2250033 ITC-Nexus Dx |
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