Medical Device Recalls
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1 result found
510(K) Number: K202000 |
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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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Silatrix Oral Gel Polymerized Sucralfate Gel 10% (1 gm/10 gm | 2 | 04/04/2022 | SA3, LLC |
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