Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K090511 |
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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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BEQ-HMO 71000-USA /QUADROX-i Adult, Oxygenator used during cardiopulmonary bypass Item no. 70106782... | 2 | 05/26/2023 | Maquet Medical Systems USA |
QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator; QUADROX-i ADULT HMO 70000 / HMO 71000; QUADROX-i... | 2 | 09/20/2013 | Maquet Cardiovascular Us Sales, Llc |
QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator; QUADROX-i ADULT HMO 70000 / HMO 71000; QUADROX-i... | 2 | 10/26/2012 | Maquet Cardiovascular Us Sales, Llc |
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