Medical Device Recalls
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1 result found
510(K) Number: K202665 |
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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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ECHELON FLEX Powered Plus Stapler-intended for transection, resection, and/or creation of anastomose... | 2 | 08/19/2021 | Ethicon Endo-Surgery Inc |
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