Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K160651 |
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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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Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281) | 2 | 11/18/2017 | Medtronic Inc. |
BD FlowSmart Set MiniMed Pro-set Rx Only Distributed by Medtronic MiniMed Inc. 8006464633 81857... | 2 | 05/01/2017 | Becton Dickinson & Company |
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