Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K123370 |
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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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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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