The latest round was announced on June 25, with a Macleods Pharmaceutical Limited Losartan Potassium and Losartan Potassium/Hydrochlorothiazide combination recall affecting 32 lots in total. This prompted the first recall of valsartan medicines due to the presence of a cancer-causing substance called N-nitrosodimethylamine (NDMA) in July 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 tablets, that contain losartan, an angiotensin II receptor blocker (ARB), and hydrochlorothiazide, a diuretic, used in combination for the treatment of hypertension. Recently, the FDA issued a recall for blood pressure medication irbesartan, also because of a NDEA contamination concern. The substance is a probable human carcinogen, according to the International Agency for Research on Cancer. Patients with questions about the recall can contact Sandoz Inc. at 800-525-8747 or email usdrugsafety.operations@novartis.com. Torrent Pharmaceuticals Ltd. has expanded its recall of losartan potassium and losartan potassium/hydrochlorothiazide tablets. Losartan Recall . The Sandoz Inc. recall involved 100 milligram/25 milligram Losartan tablets with the lot number JB8912 and expiration date of June 2020. Search List of Recalled Angiotensin II Receptor Blockers (ARBs) including Valsartan, Losartan and Irbesartan. The active pharmaceutical ingredient (the real medicine) was made in China by Zhejiang Huahai Pharmaceutical Co. Ltd., the same Chinese company that made the contaminated valsartan. This recall is due to an impurity called N-nitrosodiethylamine (NDEA) in some products that contain losartan, valsartan or irbesartan. Distribution of generic Zantac halted 03:00. Torrent Pharmaceuticals says two of its blood pressure medications were found to have trace amounts of a potentially cancer … Torrent Pharmaceuticals Limited has again expanded a recall of its blood pressure medication over concerns the tablets contain small amounts of a cancer-causing ingredient. Quotes displayed in real-time or delayed by at least 15 minutes. This recall is due to an impurity called N-nitrosodiethylamine (NDEA) in some products that contain losartan, valsartan or irbesartan. Powered and implemented by FactSet Digital Solutions. “The risk of developing cancer in a few patients following long-term use of the product cannot be ruled out,” the FDA noted. Valsartan is a similar blood pressure medication to losartan. This material may not be published, broadcast, rewritten, or redistributed. Many patients that were on Valsartan were switched over to Losartan after Valsartan was recalled in July 2018. Legal Statement. The recall of a widely-prescribed blood pressure drug losartan is being expanded again by the Food and Drug Administration due to contamination by cancer-linked chemical. MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. A widespread recall of common blood pressure and heart failure medications has been expanded to include more drugs containing losartan due to an "impurity" that may pose a cancer risk. Over the summer, blood pressure drug valsartan was similarly recalled. Hundreds of lots of losartan drugs and others in its class have been recalled by more than a dozen drug manufacturers since impurities were first discovered in mid-2018. Contact a Sullo & Sullo hydrochlorothorazide lawyer today, for highly qualified legal assistance with your amlodipine recall lawsuit. Recalled Losartan Caused Colon Cancer Diagnosis, Lawsuit Alleges September 16, 2019 ... Side effects of Belviq may increase the risk of cancer, resulting in a diet drug recall and lawsuits. Legal Statement. It is an animal and human carcinogen. Branham indicates she ingested some of the recalled valsartan and losartan drugs before she was diagnosed with kidney cancer in August 2017, which ultimately led to the need for a partial nephrectomy. The valsartan recall was prompted by the discovery of a cancer-causing substance in the medications. Note: This story was updated on Sept. 23, 2019, with an additional losartan recall from Torrent Pharmaceuticals. The U.S. Food and Drug Administration announced a third blood pressure medication recall over concerns the contaminated drug might cause cancer. Losartan Recall – What is the Cancer-Causing Ingredient It was indicated that Losartan tablets contain N-methylnitrosobutyric acid (NMBA). BLOOD PRESSURE MEDICATION RECALL EXPANDED OVER POSSIBLE CANCER-CAUSING INGREDIENT . The recall involves losartan and potassium/hydrochlorothiazide combination pills found to contain N-Nitroso-N-methyl-4-aminobutyric acid, or NMBA, according to a … You've successfully subscribed to this newsletter! Check out what's clicking on Foxnews.com. A recall for blood pressure drugs has been expanded. Losartan Recall Lawsuit. ©2021 FOX News Network, LLC. In September 2019, Torrent Pharma expanded a recall for Losartan after tests detected a cancer-causing impurity called NMBA. Market data provided by Factset. Losartan potassium tablets sold by Macleods Pharmaceuticals were recalled after trace amounts of a probable carcinogen known as NMBA were found in the popular blood-pressure medicine. In November 2018, the FDA issued a recall of Losartan after detecting trace amounts of the probable human carcinogen N-nitrosodiethylamine (NDEA). Camber Pharmaceuticals, Inc. is recalling 87 lots of Losartan Tablets USP 25 mg, 50 mg, and 100 mg to consumer level. Torrent Pharmaceuticals Ltd. has expanded its recall of losartan potassium and losartan potassium/hydrochlorothiazide tablets. All rights reserved. Losartan is used to treat high blood pressure (hypertension). Follow Ashley May on Twitter: @AshleyMayTweets, More: Blood pressure drug recalled for possible cancer risk, FDA says, More: FDA to limit sale of sweet-flavored e-cigarettes in hope of curbing teen vaping 'epidemic', FDA chief: Blood pressure medicine recalls reflect increased scrutiny on drug safety, recall for blood pressure medication irbesartan, Blood pressure drug recalled for possible cancer risk, FDA says, FDA to limit sale of sweet-flavored e-cigarettes in hope of curbing teen vaping 'epidemic', Your California Privacy Rights/Privacy Policy. Losartan Recall Lawsuit. A widespread recall of common blood pressure and heart failure medications has been expanded to include more drugs containing losartan due to an "impurity" that may pose a cancer … Fox News Flash top headlines for Sept. 24 are here. losartan FDA Alerts. The company stated that the affected products found to include more NMBA than the FDA allowed. Company Announcement. The U.S. Food and Drug Administration announced a third blood pressure medication recall over concerns the contaminated drug might cause cancer. The recall was prompted by the discovery of cancer-causing impurities in the medications. The fourth was announced in April. Update [6/26/2019] FDA is alerting patients and health care professionals to Macleods Pharmaceuticals’ voluntary recall of two lots of losartan potassium tablets (50mg strength) and 30 lots of losartan potassium/hydrochlorothiazide (HCTZ) combination tablets (12 lots of 50mg/12.5mg strength, three lots of 100mg/12.5mg strength, and 15 lots of 100mg/25mg … Discussion of the losartan recall and the associated cancer risk. The recall affects Losartan Potassium tablets USP in 25, 50 and 100 mg doses. Market data provided by Factset. Many patients that were on Valsartan were switched over to Losartan after Valsartan was recalled in July 2018. A recall on losartan medications soon followed. Madeline Farber is a Reporter for Fox News. or redistributed. Following is a list of possible medication recalls, market withdrawals, alerts and warnings. Sandoz Inc. is voluntarily recalling losartan potassium hydrochlorothiazide tablets because the pills could contain an impurity N-nitrosodiethylamine (NDEA). NDEA can cause cancer, even in small amounts. The expanded recall includes an additional three lots of losartan potassium tablets USP and two lots of losartan potassium/ydrochlorothiazide … Sandoz Inc. is voluntarily recalling losartan potassium hydrochlorothiazide tablets because the pills could contain an impurity N-nitrosodiethylamine (NDEA). Quotes displayed in real-time or delayed by at least 15 minutes. NDEA appears to cause cancer in animals and is suspected to cause cancer in humans, according to lab tests. Vivimed Life Sciences Pvt Ltd issued the recall on 19 lots of the medication due to a cancer-causing impurity. More: FDA chief: Blood pressure medicine recalls reflect increased scrutiny on drug safety. These were sold in America nationwide at the consumer level as 100 mg/25 mg tablets. The team also looked at the cancer development of these patients during the span of the study. Now people who have developed cancer after taking Losartan may be able to file lawsuits. Summary: Bladder cancer is found among people who take Losartan, especially for people who are male, 60+ old, have been taking the drug for 1 - 2 years. Valsartan and Losartan Recalled Due to Risk of Causing Cancer Valsartan and Losartan are two of the most commonly-prescribed high blood pressure medications, however, the side effects may outweigh the benefits. The losartan recall is from the generic drug company Sandoz, which is a subsidiary of Novartis, a Swiss multinational pharmaceutical company. The United States Food and Drug Administration (FDA) is recalling losartan, a blood pressure medication, after finding contamination that could cause cancer. 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