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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K020813
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Product Description
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FDA Recall
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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.