Medical Device Recalls
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1 result found
510(K) Number: K855135 |
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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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BD BBL Sensi Disc Cefaclor - 30 ug®, used for semi-quantitative in vitro susceptibility testing. Cat... | 2 | 02/08/2024 | Becton Dickinson & Co. |
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