Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K140208 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016A So... | 1 | 07/10/2025 | Edwards Lifesciences, LLC |
| Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018A So... | 1 | 07/10/2025 | Edwards Lifesciences, LLC |
| Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016AS S... | 1 | 07/10/2025 | Edwards Lifesciences, LLC |
| Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018AS So... | 1 | 07/10/2025 | Edwards Lifesciences, LLC |
| Edwards Lifesciences Femoral Venous Cannula, 20F X 55CM, resterilized. | 2 | 09/13/2018 | SPS Sterilization, Inc |
| Edwards Lifesciences Femoral Venous Cannula, 18FR, resterilized. | 2 | 09/13/2018 | SPS Sterilization, Inc |
| Edwards Lifesciences Fem-Flex II Femoral Arterial Cannula 8, 10, 12 French,Sterile EO, Rx Only, Manu... | 2 | 04/02/2015 | Edwards Lifesciences, LLC |
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