Medical Device Recalls
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1 result found
510(K) Number: K020931 |
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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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BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle is intended to be recover an... | 2 | 01/25/2013 | bioMerieux, Inc. |
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