Patients should contact their pharmacist or physician who can advise them about an alternative treatment prior to returning their medication. Nov. 13, 2018 -- Yet another blood pressure drug has been recalled because of fears of impurities added by a lab in China.. Drug company Sandoz says it has recalled one lot of losartan … The recall has targeted losartan potassium tablets and losartan potassium/hydrochlorothiazide tablets. Sandoz is on Twitter. (I was also on Cozaar and then Avapro). Patients should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using Losartan Potassium Hydrochlorothiazide. There can be no guarantee that the investigational or approved products described in this press release will be submitted or approved for sale or for any additional indications or labeling in any market, or at any particular time. The recall covers 25 mg, 50 mg and 100 mg dosages. What Losartan Has Been Recalled? Recall of 3 brands of Losartan Medicines Frequently Asked Questions 1. The top-rated diet designed to lower your blood pressure. A company that presumably just started making hand sanitizer recently has been forced to recall its product due to the presence of methanol. Now, almost a year later, manufacturer Torrent Pharmaceuticals expands its voluntary recall for the 5th time. the Food and Drug Administration's website, one lot of the losartan combination drug in February, Apple voluntarily recalling batteries on MacBook Pro notebooks due to safety risk, Fisher-Price recalls 4.7 million infant sleepers after reported death, Your California Privacy Rights/Privacy Policy, BLK719A, BLK720A, BLK721A, BLK722A, BLK723A, BLK724A, September 2019, BLM825A, BLM826A, BLM827A, September 2021. What Losartan Has Been Recalled? The Ministry of Health (MOH) said that about 137,000 patients in Singapore are using the three recalled brands of losartan. Related recalls 2020-12-22 - Certain Assala, Compliments, The Deli-Shop, and Levitts brands deli meat products recalled due to … Our portfolio of approximately 1000 molecules, covering all major therapeutic areas, accounted for 2017 sales of USD 10.1 billion. Sunshine Mills, Inc. has chosen to expand its voluntary recall to include these additional products as a precautionary measure in furtherance of its commitment to the safety and quality of its products. Another 35 lots of heart and blood pressure medication losartan have been recalled because of unsafe amounts of NMBA in the active ingredient. Losartan Potassium Hydrochlorothiazide Tablets, USP are indicated for the treatment of hypertension. The active drug ingredient was manufactured at Hetero Labs Limited in India, one of the overseas drug factories linked to repeated blood medication recalls since last July. Camber Pharmaceuticals, Inc. has recalled 87 lots of Losartan Tablets USP. All 3 medicines contain losartan, an angiotensin II receptor blocker (ARB) commonly uused to treat hypertension. Before sharing sensitive information, make sure you're on a federal government site. Teva is recalling lots of losartan-containing medication that tested positive for NMBA above 9.82 parts per million. 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. Torrent Pharmaceuticals Limited has expanded its voluntary recall of Losartan potassium tablets USP to include 6 lots of Losartan potassium and hydrochlorothiazide tablets, USP. The Ministry of Health (MOH) said that about 137,000 patients in Singapore are using the three recalled brands of losartan. Here’s what to watch out for. The affected product was not distributed prior to October 8, 2018. Teva is recalling lots of losartan-containing medication that tested positive for NMBA above 9.82 parts per million. We contribute to society’s ability to support growing healthcare needs by pioneering novel approaches to help people around the world access high-quality medicine. ", MacBook Pro recall: Apple voluntarily recalling batteries on MacBook Pro notebooks due to safety risk, Rock 'n Play recall: Fisher-Price recalls 4.7 million infant sleepers after reported death. The recalled losartan potassium and losartan potassium/hydrochlorothiazide tablets are also manufactured by Hetero, which are distributed by Camber, and contain the impurity NMBA. Such forward-looking statements are based on our current beliefs and expectations regarding future events, and are subject to significant known and unknown risks and uncertainties. Recalled by Thomson International, Inc. The FDA has compiled a list of all the … The Food and Drug Administration has recently recalled a number of … A carcinogen is something that could cause you to … Losartan (blood pressure med) has been recalled by the FDA. I was on the brand name Toprol XL for about 5 years and never had a problem.-200mg. "Based on the available information, the risk of developing cancer in a few patients following long-term use of the product cannot be ruled out," the recall notice states. Safety Alerts, Due to detection of NDEA (N-Nitrosodiethylamine) Impurity, An official website of the United States government, : Only three of the ten losartan products in Singapore – Hyperten, Losagen and Losartas – contain the nitrosamine impurity. Is it safe to take my Losartan by Lupin, the one mfg by Torrent has traces of some cancer causing substance. Your healthcare provider has been advised to make arrangements to review and provide you with alternatives or other therapies. On April 24, the company recalled an additional lot of 50mg losartan tablets. Company Announcement. I was on the brand name Toprol XL for about 5 years and never had a problem.-200mg. Instructions for returning recalled products are provided in … Of these, about 130,000 patients have been … (I was also on Cozaar and then Avapro). Sign up to follow @Sandoz_global at http://twitter.com/Sandoz_Global. Doctor's Assistant: The Doctor can help. Distributors and retailers that have product which is being recalled should immediately stop distribution of the identified lot above and quarantine any quantities remaining in your control and return the recalled product to the identified Reverse Distributor. My Losartan is mfg by Lupin. Promoted by the National Heart, Lung, and Blood Institute, this diet has consistently been cited as a great plan to lower blood pressure, improve heart health, and lose weight. Worldwide blood pressure medicine recall expanding. FDA: Blood pressure medication Losartan recalled due to cancer concern. In addition to the three recalled brands, there are seven other brands of losartan medicines marketed in Singapore. The recall was first announced in January. According to the FDA, NDEA occurs naturally in certain foods, drinking water, air pollution and industrial processes, and has been classified as a probable human carcinogen. Sandoz has recalled one lot of losartan products made at its Lek Pharmaceuticals plant in Slovenia. Patients who are on Losartan Potassium Hydrochlorothiazide should continue taking their medication, as the risk of harm to a patient’s health may be higher if the treatment is stopped immediately without any alternative treatment. Sandoz Inc. is voluntarily recalling one lot of Losartan Potassium Hydrochlorothiazide Tablets, USP 100mg/25mg to the consumer level. Camber Pharmaceuticals, Inc. has recalled 87 lots of Losartan Tablets USP. We have collected all the losartan recall information in the expandable table below. Torrent Pharmaceuticals Limited is expanding its recall of Losartan potassium tablets USP due to the … Sandoz Inc. is notifying its distributors by letter via overnight mail and patients by this public notification. Additionally, Legacy expanded its recall to include one additional lot of losartan tablets made with API manufactured by Hetero Labs. Recalls, Market Withdrawals, & Safety Alerts, Recalls, Market Withdrawals and Safety Alerts, Recalls, Market Withdrawals, & Safety Alerts, Archive for Recalls, Market Withdrawals & Safety Alerts, Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient (API), Recent Recalled Product Photos on FDA's Flickr Photostream. The product can be identified as Losartan Potassium Hydrochlorothiazide, 100 mg/25 mg tablets in 1000-count plastic bottles, NDC 0781-5207-10, Lot number JB8912; Exp. The Health Sciences Authority (HSA) of Singapore is recalling three brands of blood pressure medicines. Torrent Pharmaceuticals Ltd. has expanded its recall of losartan potassium and losartan potassium/hydrochlorothiazide tablets. About Sandoz The FDA is recalling losartan, a blood pressure drug made by Sandoz, due to possible cancer concerns after contamination by the chemical NDEA was found. Forward-looking statements can generally be identified by words such as “potential,” “can,” “will,” “plan,” “expect,” “anticipate,” “look forward,” “believe,” “committed,” “investigational,” “pipeline,” “launch,” or similar terms, or by express or implied discussions regarding potential marketing approvals, new indications or labeling for the investigational or approved products described in this press release, or regarding potential future revenues from such products. Torrent Pharmaceuticals voluntarily recalled two lots of losartan potassium tablets because of trace amounts of an impurity that has been found … Brand: Pacific Gold; Sold only in Arizona, California, Nevada, and Utah stores; Walmart external icon – red, white, yellow, and sweet yellow onions. In particular, our expectations regarding such products could be affected by, among other things, the uncertainties inherent in research and development, including clinical trial results and additional analysis of existing clinical data; regulatory actions or delays or government regulation generally; global trends toward health care cost containment, including government, payor and general public pricing and reimbursement pressures; our ability to obtain or maintain proprietary intellectual property protection; the particular prescribing preferences of physicians and patients; general political and economic conditions; safety, quality or manufacturing issues; potential or actual data security and data privacy breaches, or disruptions of our information technology systems, and other risks and factors referred to in Novartis AG’s current Form 20-F on file with the US Securities and Exchange Commission. The FDA initiated what would become its largest class I drug recall to date in July 2018 and has since expanded the number of contaminated products involved. The recall is due trace amounts of an unexpected impurity, N-Methylnitrosobutyric acid (NMBA), detected during testing. For the latest recall information as of September 25, 2019 check here: New Recall Expansion Announced for Certain Losartan Products A recall of Torrent Pharmaceuticals Limited’s Losartan Potassium Tablets USP has been expanded to include 8 additional lots. Torrent and Hetero/Camber are only recalling lots of losartan-containing medication with NMBA above the interim acceptable intake limits of 0.96 parts per million (ppm). Then my new coverage was not covering so doctor switched me to Coreg CR-80mg- it seemed to work, although BP was a little elevated. STOCK PHOTO/Getty Images. Macleods also recalled one lot of the losartan combination drug in February for the same reason. Of these, about 130,000 patients have been … These brand name medications contain the active ingredients valsartan, losartan, or irbesartan, and are used to treat high blood pressure in millions of Americans. If you're concerned you may be taking recalled losartan, compare the information on your prescription drug label with the information in the table. The mfg. In December 2018, Torrent Pharmaceuticals began a voluntary recall of losartan due to the presence of small traces of known carcinogens. Consumers with medical questions or to report an adverse event can contact Macleods at 855-926-3384 from 8 a.m. to 5 p.m. EST. Blood Pressure Medicine Is Recalled - The New York Times. 34 Related Question Answers Found Is losartan dangerous? Torrent is recalling 10 lots of losartan-containing products which have been found to contain N-nitrosodiethylamine (NDEA) above the acceptable daily intake levels. Dozens of blood pressure medications have been recalled since the first products were pulled off the shelf in July 2018 due to impurities. Image. Legacy Pharmaceutical Packaging LLC is notifying its distributors and customers in writing and is arranging/assisting for the return of all recalled products to Inmar Pharmaceutical Services. Patients with questions regarding this recall can contact Sandoz Inc. at 1-800-525-8747 Monday-Friday 8:30 AM – 5:00 PM (EST) or email usdrugsafety.operations@novartis.com. There has been a recall on Metroprolol. No illnesses have been reported in association with these products to date, and no other Sunshine Mills, Inc. pet food products are affected by this announcement. The recall was issued due to the detection of trace amounts of an unexpected impurity found in an active pharmaceutical ingredient (API) manufactured by Hetero Labs Limited. The recalled losartan and potassium/hydrochlorothiazide combination tablets contained small amounts of N-nitrosodiethylamine, or NDEA, according to a company notice posted to the Food and Drug Administration's website Wednesday. Novartis is providing the information in this press release as of this date and does not undertake any obligation to update any forward-looking statements contained in this press release as a result of new information, future events or otherwise. Macleods Pharmaceuticals Limited is recalling 32 lots of the popular blood pressure drug losartan after discovering trace amounts of a probable carcinogen. (FiercePharma) FDA losartan recall: Cancer risk tied to blood pressure drug losartan. Which are the high blood pressure medicines recalled by the Health Sciences Authority? Your healthcare provider has been advised to make arrangements to review and provide you with alternatives or other therapies. Legacy Pharmaceutical Packaging LLC is notifying its distributors and customers in writing and is arranging/assisting for the return of all recalled products to Inmar Pharmaceutical Services. The Health Sciences Authority (HSA) has recalled three brands of high blood pressure medicine which contain losartan – Losartas, Losagen and Hyperten – on 28 March 2019. Low levels of nitrosamines, which are environmental contaminants, may be found in water and … This product is … Nov. 13, 2018 -- Yet another blood pressure drug has been recalled because of fears of impurities added by a lab in China.. Drug company Sandoz says it has recalled one lot of losartan … ... To determine if you're medication has been recalled… The site is secure. Why Has Valsartan Been Recalled? Sandoz has recalled one lot of losartan products made at its Lek Pharmaceuticals plant in Slovenia. To date, Sandoz Inc. has not received any reports of adverse events related to this lot. More Recalls, Market About one-third of Americans have chronic high blood pressure, making it one of the most common health conditions in the United States.Recently, popular medications to treat high blood pressure have been under scrutiny by the FDA for containing cancer-causing impurities.. Another blood pressure medication has been recalled over concerns it could contain trace amounts of carcinogens. They were found to contain higher than accepted levels of a nitrosamine impurity, N-nitroso-N-methyl-4-aminobutyric acid (NMBA). January 28, 2019 at 9:45 am EST By Natalie Dreier, Cox Media Group National Content Desk. The company said in the statement that for this recall "it has not received any reports of … Recalled by Progressive Produce, LLC. 4 Losartan belongs to a class of medicines called angiotensin II receptor blockers (ARBs), which are used to treat high blood pressure, also known as hypertension. Torrent Pharmaceuticals Limited has expanded its recall of Losartan potassium tablets USP. Tests found trace amounts of … (FiercePharma) FDA losartan recall: Cancer risk tied to blood pressure drug losartan. Originally the company recalled 10 lots of the medication. There has been a recall on Metroprolol. Macleods also recalled one lot of the losartan combination drug in February for the same reason. Over 50 Companies Have Recalled Losartan, Valsartan Since July. One lot of Losartan tablets, used to treat high blood pressure, has been recalled by Sandoz because it includes “a trace amount” of N-nitrosodiethylamine, commonly referred to as NDEA. Legacy Pharmaceutical Packaging, LLC on March 15 recalled 43 lots of losartan tablets. The recall of Losartan is linked to a possible cancer-causing element known as NMBA. Fred Meyer external icon – cheese dips and spreads The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. This recall is being made with the knowledge of the Food and Drug Administration. However, there has been one reported illness that may be associated with the consumption of the products included in the Food Recall Warning of December 7, 2020. The recalled losartan potassium and losartan potassium/hydrochlorothiazide tablets are also manufactured by Hetero, which are distributed by Camber, and contain the impurity NMBA. This press release contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. FDA does not endorse either the product or the company. As a division of the Novartis Group, our purpose is to discover new ways to improve and extend people’s lives. They were manufactured by these drug companies: According to the FDA , about 300 lots of losartan and losartan/hydrochlorothiazide products have been recalled as of April 18, 2019. Here are the doses, lot numbers and expiration dates of the recalled medicine: Losartan Potassium and Hydrochlorothiazide Tablets 50 mg/ 12.5 mg: Losartan Potassium and Hydrochlorothiazide Tablets 100 mg/ 12.5 mg: How to make sure your blood pressure meds are safe. When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. It may be used alone or in combination with other antihypertensive agents. Valsartan, Losartan & Irbesartan Recalled Due to Cancer Risk The U.S. Food and Drug Administration (FDA) is recalling a number of high blood pressure medications over potential cancer risks. Only three of the ten losartan products in Singapore – Hyperten, Losagen and Losartas – contain the nitrosamine impurity. The initial recall of Losartan has been expanded, according to the FDA. Recalled Foods Containing Recalled Onions. Macleods Pharmaceuticals Limited is recalling 32 lots of the popular blood pressure drug losartan after discovering trace amounts of a probable carcinogen. Torrent and Hetero/Camber are only recalling lots of losartan-containing medication with NMBA above the interim acceptable intake limits of 0.96 parts per million (ppm). These seven brands have been tested by HSA and Instructions for returning recalled products are provided in … Which losartan products were recalled? Discontinuing a recalled drug could cause more immediate harm than staying on the medication. Robert Moore. Nor can there be any guarantee that such products will be commercially successful in the future. Follow our blog at www.sandoz.com/makingaccesshappen. What brand of losartan has been recalled? January 28, 2019 at 9:45 am EST By Natalie Dreier, Cox Media Group National Content Desk. This product is being recalled due to the trace amount of an impurity, N-nitrosodiethylamine (NDEA) contained in the API Losartan, USP manufactured by Zhejiang Huahai Pharmaceutical Co. Ltd. Sandoz Inc. Losartan Potassium Hydrochlorothiazide product is manufactured by Lek Pharmaceuticals dd, Ljubljana, Slovenia. Exit Full Screen. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those set forth in the forward-looking statements. The recall was issued due to the detection of trace amounts of an unexpected impurity found in an active pharmaceutical ingredient (API) manufactured by Hetero Labs Limited. Losartan, irbesartan, and other “-sartan” drugs are also part of this class of drugs. A total of 10 lots are now being recalled at the consumer level, including 2 recalled lots initially announced December 20, 2018. The U.S. Food and Drug Administration (FDA) has recalled numerous lots of valsartan. Then my new coverage was not covering so doctor switched me to Coreg CR-80mg- it seemed to work, although BP was a little elevated. Losartan and irbesartan have also been recalled due to concerns that the high blood pressure medications are contaminated with nitrosamine impurities. The pills have been flagged for … For questions about returning the product, contact Qualanex via email at recall@qualanex.com or call 888-280-2046 from 7 a.m. to 4 p.m. CST weekdays. FDA: Blood pressure medication Losartan recalled due to cancer concern. Sandoz is headquartered in Holzkirchen, in Germany’s Greater Munich area. I never had a problem until this new doctor switched me to generics in October of 2010. This product was distributed nationwide to distributors. Withdrawals, & The recall comes amid a larger string of recalls of blood pressure medications valsartan, losartan and irbesartan that contain trace levels of carcinogens … The recalled lots of Losartan were manufactured by Zhejiang Huahai Pharmaceutical Co. Ltd., the same company that manufactured the NDMA -contaminated Valsartan. Another 19 lots of losartan tablets, these made by Vivimed Life Sciences and distributed by Heritage Pharmaceuticals, have been recalled for exceeding the FDA allowable amount of NMBA. Consult your healthcare provider if you are unsure if you are taking an affected brand. What brand of losartan has been recalled? Just … The FDA has compiled a list of all the contaminated blood pressure medications. Finally, her doctor suggested valsartan from a manufacturer that has not been affected by recalls — but Brown said on Thursday that she’d learned even that lot of the drug had been recalled. Torrent Pharmaceuticals Limited has expanded its voluntary recall of Losartan potassium tablets USP to include 6 lots of Losartan potassium and hydrochlorothiazide tablets, USP. The company said in the statement that for this recall "it has not received any reports of adverse effects. This impurity, which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, has been classified as a probable human carcinogen as per International Agency for Research on Cancer (IARC). This is the fifth time in 2019 that Torrent Pharmaceuticals has expanded its voluntary recall of losartan. Additionally, Legacy expanded its recall to include one additional lot of losartan tablets made with API manufactured by Hetero Labs. Over 2 million Americans received notices in the mail alerting them of … The Food and Drug Administration posted information on its website listing the blood pressure medications recalled for containing carcinogens. 1 Consult your healthcare provider if you are unsure if you are taking an affected brand. In 2017, our products reached more than 500 million patients. The .gov means it’s official.Federal government websites often end in .gov or .mil. Herald Staff [email protected] A massive recall of some of the world’s leading brands of hypertension medication continues. Losartan is now the third “sartan” drug that has been recalled after the carcinogen N-Nitrosodiethylamine (NDEA) was detected in its active pharmaceutical ingredient. Disclaimer Sandoz Inc. is voluntarily recalling one lot of Losartan Potassium Hydrochlorothiazide Tablets, USP 100mg/25mg to the consumer level. Health care professionals advise patients to consult with their doctors or pharmacists before discontinuing one of the recalled blood pressure medicines or finding an alternative treatment. You should not place undue reliance on these statements. Adverse reactions or quality problems associated with the use of this product may be reported to FDA's MedWatch Adverse Event Reporting program either by phone, on line, by regular mail or by fax. Sandoz is a global leader in generic pharmaceuticals and biosimilars. Torrent in particular. Date 06/2020. The recall covers 25 mg, 50 mg and 100 mg dosages. Losartan Potassium was distributed by pharmacies nationwide. Losartan Potassium was distributed by pharmacies nationwide. Torrent Pharmaceuticals has announced a new expansion of its recall for Losartan Potassium Tablets USP and Losartan Potassium/hydrochlorothiazide tablets, USP to the consumer level. Blocker ( ARB ) commonly uused to treat hypertension products reached more than 500 patients! 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