Lisinopril Recall. Lupin Pharmaceuticals initiated the recall April 20, 2020. Blood pressure medication recall: What you need to know The FDA continues to update the list of medications being recalled. FDA expands recall on blood pressure drug 02:42. 1/22). The recall affects lisinopril and hydrochlorothiazide tablets, 20 mg/12.5 mg, in 500-count bottles (NDC 68180-519-02) from lot H801815 (Exp. Lupin, Sun Pharma recall Lisinopril and Clonazepam respectively in the US market. From readiness assessment and procedure development to regulatory guidance and reporting, we help minimize the possible impacts of market actions — on customers and your bottom line. CLASS II Acetaminophen and codeine phosphate tablets; 300 mg/15 mg, 300 mg/30 mg or 300 mg/60 mg; 10-, 12-, 14-, 15-, 16-, 20-, 30-, 60- or 100-count bottle. Lisinopril is used to treat high blood pressure (hypertension) in adults and children who are at least 6 years old. The recall affects lisinopril tablets, 20 mg, 1000-count bottles (NDC 68180-0981-03) from lot Q000255 (Exp. The recall was included in the April 29, 2020, US Food and Drug Administration (FDA) Enforcement Report. The FDA announced that Lupin Pharmaceuticals has pulled a lot of its lisinopril 20mg and hydrochlorothiazide 12.5mg tablets, following a complaint regarding a foreign drug tablet. ACE stands for angiotensin converting enzyme. 3/21). The previous year, Wockhardt recalled its 5mg and 20mg tablets for the same reason. If a recall does relate to the version of the drug you are taking, you should not stop taking the drug until you discuss an alternative treatment with your doctor or pharmacist. The bottles were distributed throughout the United States. Important information A recall is a voluntary action taken by a company at any time to remove a defective drug product from the market. According to the IMS Institute there were 102 million prescriptions for lisinopril in 2013, making it the third most prescribed drug in the U.S. Lisinopril has been … Reduce risk and limit exposure with our world-class market action/recall and product withdrawal services. Lisinopril is an ACE inhibitor. As of August 2016, the FDA has banned three of … In 2016, Lupin Pharmaceuticals Inc recalled 30mg and 40mg bottles of Lisinopril tablets as a result of contamination during manufacturing. The product was distributed throughout the United States. Editor’s note: This story on the recall of certain blood pressure medications has been updated numerous times since it was first published on July 24, 2018. What is lisinopril? At press time, the FDA had not yet classified the recall. The first recall was in July 2018 when China's Zhejiang Huahai Pharmaceuticals recalled batches of valsartan for trace amounts of NDMA. By Dr. Tulsie N. Patel and Dr. Sumir Shah Lupin Pharmaceuticals voluntarily initiated the recall July 19, 2019. Lisinopril, sold under the brand names Prinivil and Zestril, is an ACE inhibitor used to treat high blood pressure, treat heart failure, and improve survival after heart attack. Manufacturer Wockhardt has issued a voluntary recall of four lots of generic lisinopril (Zestril, Prinivil), an ACE inhibitor used to help lower blood pressure and treat heart failure.. Lisinopril is also used to treat congestive heart failure in adults, or to improve survival after a heart attack.