Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K020813 |
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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® FA, bioM®rieux, Inc., Product Usage: BacT/ALERT® Culture Bottles are used with the B... | 2 | 02/04/2016 | bioMerieux, Inc. |
BacT/ALERT - FA Reagent Bottle The BacT/ALERT Microbial Detection System is used to determine if mi... | 2 | 05/24/2011 | bioMerieux, Inc. |
BacT/ALERT® FA Culture Bottles, 30 ml, for in vitro diagnostic use, BioMerieux, Inc., Durham, NC 277... | 2 | 03/22/2007 | bioMerieux, Inc. |
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