Medical Device Recalls
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1 result found
510(K) Number: K030531 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medtronic MiniMed Paradigm Model 712 | 3 | 06/25/2015 |
FEI # 3003166194 Medtronic MiniMed |
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