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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
Related Medical Device Recalls Date Classified to: 09/16/2014
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Product Description
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Z-1894-2008 - Edwards Lifesciences LLC, Fem-Flex II Duraflo Treated Femoral Venous Catheter, 8 Fr. x 11.5 cm, REF DIIFEMII008V, Cardiopulmonary bypass tubing. 2 Sep-11-2008 Edwards Lifesciences Research Medical, Inc.
Z-1893-2008 - Edwards Lifesciences LLC, Fem-Flex II Femoral Venous Cannula, 12 Fr. x 11.5 cm, REF FEMII012V, Cardiopulmonary bypass tubing. 2 Sep-11-2008 Edwards Lifesciences Research Medical, Inc.
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