Medical Device Recalls
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1 result found
510(K) Number: K931962 |
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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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Covidien Endo Peanut 5mm Auto Suture Blunt Dissector Item Code: 173019 The instrument has indicati... | 2 | 06/23/2017 | Covidien LLC |
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