美敦力胰岛素泵再陷召回风波,波科两款产品获FDA批准,维心医疗腔静脉滤器国内获批

医药经济报
Oct 27, 2024

近日,美国食品药品监督管理局(FDA)宣布,将美敦力公司召回的MiniMed 600和700系列胰岛素泵电池事件定级为最严重的I类召回,这表明使用这些设备可能会导致严重的伤害甚至死亡。美敦力公司早已关注到胰岛素泵电池寿命的问题。从2023年1月至2024年9月,该公司在美国收到了170起高血糖症(血糖水平超过400mg/dL)和11起糖尿病酮症酸中毒的报告,这些病例可能与电池问题有关。根据FDA的...

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