Medical Device Recalls
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1 result found
510(K) Number: K172361 |
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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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EEA Circular Stapler with Tri-Staple Technology, Part No. TRIEEA28MT TRIEEA28XT TRIEEA31MT TRIEEA31X... | 2 | 10/04/2018 | COVIDIEN LLC |
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