Recall Radar · 美国食品召回雷达
FDA Recalls, Market Withdrawals & Safety Alerts · Other / 其他Quinapril 20 and 40 mg tablets
Official-information notice / 官方信息说明: This page transcribes fields from the named agency record. It is not medical, legal, or food-safety advice. Follow the agency's original notice and instructions.
Recall number / 召回编号
fda-alert:2022-12-21:Lupin:Quinapril 20 and 40 mg tablets
Classification / 风险等级
Other / 其他
Published / 发布时间
2022-12-21
Recalling firm / 召回企业
Lupin Pharmaceuticals Inc.
Product description / 产品描述
Quinapril 20 and 40 mg tablets
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
Presence of nitrosamine impurity, N-Nitroso-Quinapril
Open official source ↗ / 打开官方来源
Last synchronized: 2022-12-21. Recall Radar does not replace agency guidance.