Medical Device Recalls
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31 to 31 of 31 Results
510(K) Number: K013153 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Dreamtome Cannulating Sphincterotome-DREAMTOME 44-20MM/450CM Material Number: M00584060 | 2 | 03/11/2022 | Boston Scientific Corporation |
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