Medical Device Recalls
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1 result found
510(K) Number: K033463 |
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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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Edwards Aortic Perfusion Cannula with Duraflow Coating, REF: DARH201190TA, 20 Fr. x 28 cm, Sterile E... | 2 | 05/13/2011 | Edwards Lifesciences Llc |
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