Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K031361 |
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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 21-7346-24; b) REF 21-7363-24 | 1 | 01/30/2023 | Smiths Medical ASD Inc. |
CADD Administration Sets, Model #21-7346-24 | 2 | 10/19/2021 | Smiths Medical ASD Inc. |
CADD® High Volume Administration Set with FlowStop, 21-7381-24. Product Usage: The CADD® High-V... | 2 | 10/11/2018 | Smiths Medical ASD Inc. |
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