Medical Device Recalls
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1 result found
510(K) Number: K921420 |
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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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| BD BBL Sensi Disc Azithromycin -15 ®g, Catalog Number 231682®used for semi-quantitative in vitro sus... | 2 | 02/08/2024 | Becton Dickinson & Co. |
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