Kogenate® FS antihemophilic factor (recombinant)
Official-information notice / 官方信息说明
This page organizes fields from the named agency record. It is not medical, legal, or food-safety advice. Always compare your package with the official notice.
Official record details
官方记录详情：以原始机构公告为准
Recall number / 召回编号
fda-alert:2019-07-19:Kogenate®:Kogenate® FS antihemophilic factor (recombinant)
Classification / 风险等级
Other / 其他
Published / 发布时间
2019-07-19
Recalling firm / 召回企业
Bayer
Product description / 产品描述
Kogenate® FS antihemophilic factor (recombinant)
Product code / 产品代码
Not provided in the official record
Code information / 批次与代码信息
Not provided in the official record
Product quantity / 产品数量
Not provided in the official record
Distribution / 销售地区
Not provided in the official record
Reason for recall / 召回原因
Mislabeling-contains the FVIII hemophilia A treatment, Jivi® antihemophilic factor
Need the original notice?
Open the agency source for the complete official notice and any disposal, return, or contact instructions.
← Return to Recall Radar search / 返回搜索雷达
Last synchronized: 2019-07-19. Recall Radar does not replace agency guidance.