雅培人工心脏一级召回

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器械之家医疗器械媒体报道先锋分享专业医疗器械知识关注来源:Medtech Dive 医潜美国食品药品监督管理局(FDA)近日宣布,因存在突发断电风险,对雅培公司生产的HeartMate 3和HeartMate II左心室辅助系统(LVAS)的移动电源单元(MPU)实施一级召回。这是该系列设备近年来再次因质量问题引发全球关注。召回核心:电源单元存在致命缺陷本次召回涉及2024年4月至2025年2月...

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