Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K151791 |
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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 FX25 Hollow Fiber Oxygenator, Catalog Numbers 3CX*FX25REC, 3CX*FX25RWC | 2 | 04/05/2023 | Terumo Cardiovascular Systems Corporation |
(1) Capiox FX25 (West) Advance Oxygenator- with left port, 4-liter Reservoir, XC modified to Advan... | 2 | 12/14/2020 | Terumo Cardiovascular Systems Corporation |
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