Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K110534 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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The Randox Liquid Cardiac Controls Level 1, Level 2, and Level 3 are liquid controls containing BNP,... | 2 | 12/14/2016 | Randox Laboratories |
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