Medical Device Recalls
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1 result found
510(K) Number: K090511 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BEQ-HMO 71000-USA /QUADROX-i Adult, Oxygenator used during cardiopulmonary bypass Item no. 70106782... | 2 | 05/26/2023 |
FEI # 3008355164 Maquet Medical Systems USA |
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