Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K002138 |
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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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Silhouette Paradigm 13mm, 18"; Silhouette 43"; Silhouette 23"; Silhouette Paradigm 43"; Silhouette P... | 2 | 11/03/2016 | Unomedical As |
Medtronic MiniMed Silhouette and/or MiniMed Sure-T Infusion Sets; Paradigm Silhouette infusion sets:... | 2 | 12/12/2014 | Medtronic MiniMed Inc. |
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