美国食品药品监督管理局（FDA）发布公告称，雅培糖尿病护理部门已决定召回部分型号的Freestyle Libre 3和Freestyle Libre 3 Plus传感器。此次召回行动通过官方网站对外公布，涉及产品可能存在潜在问题，但具体细节尚未披露。雅培方面表示将全力配合监管要求，确保患者安全。
美国食品药品监督管理局（FDA）发布公告称，雅培糖尿病护理部门已决定召回部分型号的Freestyle Libre 3和Freestyle Libre 3 Plus传感器。此次召回行动通过官方网站对外公布，涉及产品可能存在潜在问题，但具体细节尚未披露。雅培方面表示将全力配合监管要求，确保患者安全。
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