Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K073559 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Edwards Lifesciences Optisite Arterial Perfusion Cannula, 22F X 24CM, resterilized. | 2 | 09/13/2018 | SPS Sterilization, Inc |
| Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number... | 1 | 07/10/2025 | Edwards Lifesciences, LLC |
| Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number... | 1 | 07/10/2025 | Edwards Lifesciences, LLC |
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