Medical Device Recalls
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1 result found
510(K) Number: K081156 |
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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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CADD Administration Set, List Numbers: a) REF 21-7308-24, b) REF 21-7309-24, c) REF 21-7310-24. ... | 1 | 01/30/2023 | Smiths Medical ASD Inc. |
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