What Losartan Has Been Recalled? Just … (FiercePharma) FDA losartan recall: Cancer risk tied to blood pressure drug losartan. The FDA has compiled a list of all the … Brand: Pacific Gold; Sold only in Arizona, California, Nevada, and Utah stores; Walmart external icon – red, white, yellow, and sweet yellow onions. 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. Only three of the ten losartan products in Singapore – Hyperten, Losagen and Losartas – contain the nitrosamine impurity. Discontinuing a recalled drug could cause more immediate harm than staying on the medication. This is the fifth time in 2019 that Torrent Pharmaceuticals has expanded its voluntary recall of losartan. Sandoz is a global leader in generic pharmaceuticals and biosimilars. ", 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. Here’s what to watch out for. A carcinogen is something that could cause you to … Herald Staff [email protected] A massive recall of some of the world’s leading brands of hypertension medication continues. The recall has targeted losartan potassium tablets and losartan potassium/hydrochlorothiazide tablets. A company that presumably just started making hand sanitizer recently has been forced to recall its product due to the presence of methanol. The recall comes amid a larger string of recalls of blood pressure medications valsartan, losartan and irbesartan that contain trace levels of carcinogens … Teva is recalling lots of losartan-containing medication that tested positive for NMBA above 9.82 parts per million. It may be used alone or in combination with other antihypertensive agents. Image. The recall covers 25 mg, 50 mg and 100 mg dosages. Additionally, Legacy expanded its recall to include one additional lot of losartan tablets made with API manufactured by Hetero Labs. 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 Ministry of Health (MOH) said that about 137,000 patients in Singapore are using the three recalled brands of losartan. Robert Moore. Consult your healthcare provider if you are unsure if you are taking an affected brand. The Food and Drug Administration posted information on its website listing the blood pressure medications recalled for containing carcinogens. Torrent Pharmaceuticals Limited has expanded its voluntary recall of Losartan potassium tablets USP to include 6 lots of Losartan potassium and hydrochlorothiazide tablets, USP. All 3 medicines contain losartan, an angiotensin II receptor blocker (ARB) commonly uused to treat hypertension. 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. Macleods also recalled one lot of the losartan combination drug in February for the same reason. Camber Pharmaceuticals, Inc. has recalled 87 lots of Losartan Tablets USP. The recalled losartan potassium and losartan potassium/hydrochlorothiazide tablets are also manufactured by Hetero, which are distributed by Camber, and contain the impurity NMBA. Disclaimer 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 Food and Drug Administration has recently recalled a number of … 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. Originally the company recalled 10 lots of the medication. (I was also on Cozaar and then Avapro). I was on the brand name Toprol XL for about 5 years and never had a problem.-200mg. 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). Camber Pharmaceuticals, Inc. has recalled 87 lots of Losartan Tablets USP. 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. 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. Sandoz has recalled one lot of losartan products made at its Lek Pharmaceuticals plant in Slovenia. The initial recall of Losartan has been expanded, according to the FDA. According to the FDA , about 300 lots of losartan and losartan/hydrochlorothiazide products have been recalled as of April 18, 2019. Which losartan products were recalled? In December 2018, Torrent Pharmaceuticals began a voluntary recall of losartan due to the presence of small traces of known carcinogens. Over 50 Companies Have Recalled Losartan, Valsartan Since July. 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. Torrent Pharmaceuticals Limited is expanding its recall of Losartan potassium tablets USP due to the … Your healthcare provider has been advised to make arrangements to review and provide you with alternatives or other therapies. Recall of 3 brands of Losartan Medicines Frequently Asked Questions 1. Additionally, Legacy expanded its recall to include one additional lot of losartan tablets made with API manufactured by Hetero Labs. 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. 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. 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. This recall is being made with the knowledge of the Food and Drug Administration. Another blood pressure medication has been recalled over concerns it could contain trace amounts of carcinogens. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. Sandoz Inc. is voluntarily recalling one lot of Losartan Potassium Hydrochlorothiazide Tablets, USP 100mg/25mg to the consumer level. FDA: Blood pressure medication Losartan recalled due to cancer concern. Losartan Potassium was distributed by pharmacies nationwide. They were manufactured by these drug companies: 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. Worldwide blood pressure medicine recall expanding. 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. Macleods Pharmaceuticals Limited is recalling 32 lots of the popular blood pressure drug losartan after discovering trace amounts of a probable carcinogen. The U.S. Food and Drug Administration (FDA) has recalled numerous lots of valsartan. The recall covers 25 mg, 50 mg and 100 mg dosages. Of these, about 130,000 patients have been … To date, Sandoz Inc. has not received any reports of adverse events related to this lot. These seven brands have been tested by HSA and I was on the brand name Toprol XL for about 5 years and never had a problem.-200mg. When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. The recall is due trace amounts of an unexpected impurity, N-Methylnitrosobutyric acid (NMBA), detected during testing. 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. About Sandoz The recalled lots of Losartan were manufactured by Zhejiang Huahai Pharmaceutical Co. Ltd., the same company that manufactured the NDMA -contaminated Valsartan. 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