Medical Device Recalls
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101 to 103 of 103 Results
510(K) Number: K053404 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Edwards LifeStent FlexStar Biliary Stent System; Biliary catheter and accessories; Model Number: EX1... | 2 | 07/02/2008 | Edwards Lifesciences, Llc |
Edwards LifeStent FlexStar Biliary Stent System; Biliary catheter and accessories; Model Number: EX0... | 2 | 07/02/2008 | Edwards Lifesciences, Llc |
Edwards Lifesciences LifeStent FlexStar Bilary Stent System Application, Model EX080801CD; 8 MM x 80... | 2 | 11/28/2007 | Edwards Lifesciences, Llc |
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