Medical Device Recalls
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1 result found
510(K) Number: K842253 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Sensi Disc Amoxicillin with Clavulanic Acid 20/10 ®g, Catalog No. 231628 and 231629.® These discs... | 2 | 02/08/2024 |
FEI # 1119779 Becton Dickinson & Co. |
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