Medical Device Recalls
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1 result found
510(K) Number: K132493 |
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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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Endo GIA" Radial Reload with Tri-Staple" Technology The Endo GIA radial reloads with Tri-Staple ... | 2 | 03/06/2018 | Covidien LLC |
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