热点 来源:界面新闻 时间:2023-04-23 15:11:32
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国家药监局网站4月23日消息,碧迪医疗器械(上海)有限公司报告,由于软件问题可能导致不正确的信息处理,生产商碧迪科斯化有限公司 BD Kiestra B.V.对全自动微生物样本处理系统 BD Kiestra InoqulA+ TLA(国械备20220143)主动召回。召回级别为二级召回。
(文章来源:界面新闻)
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