Medical Device Recalls
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1 result found
510(K) Number: K983974 |
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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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Autopen Classic Automatic insulin delivery pen, 3.0ml x 2 unit 2-42 units, AN3800, Lot 7JH, NDC 0847... | 2 | 07/15/2015 | Owen Mumford USA, Inc. |
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