Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K173270 |
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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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Tri-Staple 2.0 Black Reinforced Intelligent Reload- Applications in abdominal, gynecologic, pediatr... | 2 | 05/24/2024 | Covidien, LP |
Covidien Tri-Staple 2.0 Reinforced Intelligent Reload 60 mm Medium/Thick-For use with Signia staplin... | 2 | 04/13/2021 | Covidien Llc |
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