Medical Device Recalls
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1 result found
510(K) Number: K070262 |
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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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| Oxoid Antimicrobial Susceptibility Test Discs, Ertapenem 10 mcg., CT1761B, packaged in cartridges of... | 2 | 01/21/2014 | Remel Inc |
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