Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K103191 |
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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-i Pediatric, Oxygenator used during cardiopulmonary bypass Model ... | 2 | 05/30/2023 | Maquet Medical Systems USA |
QUADROX-i Pediatric, Oxygenator used during cardiopulmonary bypass Model Ite... | 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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