Medical Device Recalls
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1 result found
510(K) Number: K872783 |
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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 Ampicillin with Sulbactam 10/10 ®g, Catalog Number 231660. Used for semi-quantit... | 2 | 02/08/2024 |
FEI # 1119779 Becton Dickinson & Co. |
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