Medical Device Recalls
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1 result found
510(K) Number: K933939 |
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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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| BacT/ALERT Blood Collection Adapter The BacT/ALERT Adapter Cap is intended for use as an aid to f... | 2 | 03/30/2012 |
FEI # 3002769706 bioMerieux, Inc. |
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