国家药监局去年发布154次召回信息 19种产品曾在国内销售

新京报
09 Jan

1月7日,国家药监局公布了最新修订的《医疗器械监督管理条例》提及,国家建立医疗器械不良事件监测制度,对医疗器械不良事件及时进行收集、分析、评价、控制;医疗器械注册人、备案人应当履行建立并执行产品追溯和召回制度等义务。召回制度被认为是产品安全的“最后一道防线”。记者梳理了2024年国家药监局发布的154次医疗器械召回信息发现,一级、二级、三级召回次数占比分别约为14.29%、44.81%、...

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