Medical Device Recalls
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1 result found
510(K) Number: K821906 |
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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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CORFLO-Ultra Jejunal Tube with CORLOCK-Twoomey Y-Adaptor for use with the CORFLO-Max PEG; enteral fe... | 2 | 02/22/2012 | Corpak Med Systems |
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