Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K062381 |
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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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CAPIOX RX15 Hollow Fiber Oxygenator, Catalog Number 3CX*RX15RE30 | 2 | 04/05/2023 | Terumo Cardiovascular Systems Corporation |
Terumo Custom Cardiovascular Procedure Kit (manufactured to the design and specifications of the pu... | 2 | 05/11/2012 | Terumo Cardiovascular Systems Corp |
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