Recall Radar · 美国食品召回雷达
FDA Recalls, Market Withdrawals & Safety Alerts · Other / 其他Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL) 100 mL
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:2024-07-22:Hikma:Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL) 100 mL
Classification / 风险等级
Other / 其他
Published / 发布时间
2024-07-22
Recalling firm / 召回企业
Hikma Pharmaceuticals PLC
Product description / 产品描述
Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL) 100 mL
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
Potential presence of Dexmedetomidine HCL Injection (400mcg/100mL) inside the overwrap that is labelled Acetaminophen Injection, 1000mg/100mL, (10mg/mL).
Open official source ↗ / 打开官方来源
Last synchronized: 2024-07-22. Recall Radar does not replace agency guidance.