Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K093522 |
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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 oxygenators Custom tubing packs for the oxygenator | 2 | 04/12/2016 | Maquet Cardiovascular Us Sales, Llc |
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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