美国食品药品监督管理局（FDA）发布公告称，ICU医疗公司正在召回其生产的静脉输液重力滴定器套装。此次召回的原因是该滴定器组件中缺少一个关键的内部截止阀，该阀门的设计功能是用于停止液体流动。这一缺陷可能导致无法有效控制药液流速，存在潜在的安全风险。
美国食品药品监督管理局（FDA）发布公告称，ICU医疗公司正在召回其生产的静脉输液重力滴定器套装。此次召回的原因是该滴定器组件中缺少一个关键的内部截止阀，该阀门的设计功能是用于停止液体流动。这一缺陷可能导致无法有效控制药液流速，存在潜在的安全风险。
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