Medical Device Recalls
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1 result found
510(K) Number: K993772 |
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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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Terumo Cardiovascular Systems CAPIOX (r) SX18 Hollow Fiber Oxygenator LOT: HF22 ®. 2010-04 The X-coa... | 3 | 01/24/2012 | Terumo Cardiovascular Corporation |
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