Medical Device Recalls
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1 result found
510(K) Number: K113411 |
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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 Lifesciences Vent Catheters, . Packaged sterile and non-pyrogenic in a sealed, peel-type pou... | 2 | 11/14/2014 | Edwards Lifesciences, LLC |
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