Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K101153 |
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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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QUADROX-iD Adult, Oxygenator used during cardiopulmonary bypass Model ... | 2 | 05/30/2023 | Maquet Medical Systems USA |
HMOD 70000-USA/QUADROX-iD Adult, Oxygenator used during cardiopulmonary bypass Item no. 701067840 | 2 | 05/26/2023 | Maquet Medical Systems USA |
BEQ-HMOD70000-USA/QUADROX-iD, Oxygenator used during cardiopulmonary bypass Item no. 701067859 | 2 | 05/26/2023 | Maquet Medical Systems USA |
QUADROX-i oxygenators Custom tubing packs for the oxygenator | 2 | 04/12/2016 | Maquet Cardiovascular Us Sales, Llc |
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