The recall is due to unacceptable amounts of N-Nitrosodiethylamine (NDEA) in the irbesartan active pharmaceutical ingredient manufactured by Zhejiang Huahai Pharmaceuticals (ZHP) in Linhai, Taizhou Zhejiang, China. Since July, medication recalls involving multiple companies and products have been announced...
FDA警示患者和卫生专业人员:山德士因NDEA召回一批氯沙坦钾氢氯噻嗪 Update [11/9/2018]FDA is alerting patients and health care professionals to Sandoz’s voluntary recall of one lot –JB8912 – of losartan potassium and hydrochlorothiazide 100mg/25mg...
The FDA advises patients to contact their doctors and possibly set up an alternative medication routine before halting their use of the drug. The full list of recalled lotscan be found on the FDA’s recall page. If you have a bottle of these tablets that match the recalled lots, contact ...
The U.S. Food and Drug Administration has expanded its recall of a commonly used type of heart drug because some of the products may contain a potentially cancer-causing chemical. Last month, the FDA issued a voluntary recall of certain batches of the drug valsartan, which is used to ...
Update: Recall of Plastic Syringes 2024年5月22日,FDA宣布江苏神力医药生产有限公司(Jiangsu Shenli Medical Production Co. 已启动召回程序,停止使用未经授权的塑料注射器。 5月23日,FDA宣布Medline Industries, LP(一家在美国境内销售和分销中国制造的塑料注射器的公司)已启动召回程序,要求停止使用受影响的产品,其中...
Recalled items come with the expiration date of August 2020. Impacted patients should contact their medical provider for advice on what to do after they learn their birth control pills were affected. On Twitter, many were reporting on the recall. RECALL: Birth control medication recalled over inco...
If you have been injured or become ill due to defective prescription medication, contact the nationally recognized product liability attorneys.
The FDA Alerts below may be specifically about Gennin-FC or relate to a group or class of drugs which include Gennin-FC. MedWatch Safety Alertsare distributed by the FDA and published by Drugs.com. Following is a list of possible medication recalls, market withdrawals, alerts and warnings....
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. STERILE PRODUCTSNDC ALUMINUM POTASSIUM SULFATE CONCENTRATED (PF) 300 G/300 ML 05446-0637-03 BUFFERED LIDOCAINE HCL (PF) 1% 05446-0850-10 BUFFERED LIDOCAINE HCL / EPINEPHRINE SOLUTION (PF) 1% / 1:100...
The U.S. Food and Drug Administration issued a voluntary recall of several medications that contain the active ingredient valsartan, which is used to treat high blood pressure and heart failure. Ad "This recall is due to an impurity, N-nitrosodimethylamine (NDMA), which was found in the reca...