Medical Device Recalls
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1 result found
510(K) Number: K933390 |
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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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Smiths Medical CADD Blue-Striped IV Administration Set, REF 21-7036-01, Sterilized using ethylene ox... | 2 | 07/24/2017 | Smiths Medical ASD Inc. |
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