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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K123370
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EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, ... 2 11/18/2019 Edwards Lifesciences, LLC
Edwards Lifesciences Aortic Perfusion Cannula, 24F x 30CM, resterilized. 2 09/13/2018 SPS Sterilization, Inc
Edwards Lifesciences EZ Glide Aortic Cannula, 24F x 37.6CM, resterilized. 2 09/13/2018 SPS Sterilization, Inc
Edwards Lifesciences Fem-Flex Femoral Arterial Cannula with Duraflo Coating, DIITFA02225, Sterile, R... 2 11/01/2013 Edwards Lifesciences, LLC
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