Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K964161 |
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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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EndoClamp aortic catheter. Label reading in part: "***CARDIOVATIONS EndoClamp aortic catheter 100 cm... | 1 | 11/06/2009 | Edwards Lifesciences Research Medical, Inc. |
EndoClamp aortic catheter label reading in part: "CARDIOVATIONS EndoClamp aortic catheter 65 cm,STER... | 1 | 11/06/2009 | Edwards Lifesciences Research Medical, Inc. |
Edwards Lifesciences CardioVations, EndoClamp aortic catheter 100 cm, REF EC1001, Sterile R, individ... | 2 | 01/05/2009 | Edwards Lifesciences Research Medical, Inc. |
CardioVations Ethicon, a Johnson and Johnson company, EndoClamp aortic catheter 100 cm, REF EC1001, ... | 2 | 01/05/2009 | Edwards Lifesciences Research Medical, Inc. |
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