Medical Device Recalls
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1 result found
510(K) Number: K142908 |
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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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Parietex Composite Parastomal Mesh (Product Number PCOPM15 / PCOPM20) Product Usage: The PCOPM15... | 2 | 11/14/2018 | Covidien LLC |
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