Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K100278 |
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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 Pediatric, Oxygenator used during cardiopulmonary bypass Model ... | 2 | 05/30/2023 | Maquet Medical Systems USA |
Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric Diffusion Membrane Oxygenator with Biolin... | 2 | 12/12/2019 | GETINGE US SALES LLC |
Maquet Quadrox-ID Pediatric Diffusion Membrane Oxygenator with Bioline Coating; Part Number BEQ-HMOD... | 2 | 12/24/2014 | Maquet Cardiovascular Us Sales, Llc |
MAQUET QUADROX iD PEDIATRIC -OXYGENATOR: BEQ-HMOD 3000; Made In Germany The diffusion membrane o... | 2 | 01/11/2012 | Maquet Cardiovascular Us Sales, Llc |
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