Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K180950 |
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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 NX19 Hollow Fiber Oxygenator, Catalog Number 3CX*NX19RE | 2 | 04/05/2023 | Terumo Cardiovascular Systems Corporation |
Terumo Capiox NX19 Oxygenator (West Orientation P/N:CXOT281 Exported only to Japan for inclusion in... | 2 | 07/30/2019 | Terumo Cardiovascular Systems Corporation |
Terumo Capiox NX19 Oxygenator (East Orientation), P/N: CXOT280 Exported only to Japan for inclusion... | 2 | 07/30/2019 | Terumo Cardiovascular Systems Corporation |
Terumo Capiox NX19 Oxygenator With Reservoir (East Orientation) P/N: 3CX*NX19RE | 2 | 07/30/2019 | Terumo Cardiovascular Systems Corporation |
Terumo Capiox NX19 Oxygenator With Reservoir (West Orientation) P/N: 3CX*NX19RW | 2 | 07/30/2019 | Terumo Cardiovascular Systems Corporation |
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