We understand that this medicine is important to your health. Aurobindo refuses to provide updated availability information. The affected lots are being recalled due to an unexpected impurity in the manufacturers’ active pharmaceutical ingredient (API). The propaganda…, A strong start to the Republican majority. The product/lots included in the expanded recall are listed below in red. The recall of Losartan is linked to a possible cancer-causing element known as NMBA. Valsartan may be linked to liver cancer, colorectal cancer, and kidney cancer. All rights reserved. Recall expansions also were announced January 3 , January 22 , March 1, and April 18. Torrent is arranging for return of all recalled products to Qualanex. Recall of metformin hydrochloride extended-release tablets 500 mg by Apotex due to N-Nitrosodimethylamine (NDMA).... Read More EDUCATION May 28, 2020 HeartWare HVAD Pump Outflow Graft and Outflow Graft Strain Relief by Medtronic Torrent Pharmaceuticals Limited has expanded its voluntary recall of losartan blood pressure medication. Losartan Potassium Hydrochlorothiazide Tablets, USP are indicated for the treatment of hypertension. Added May 2, 2020 Reason for recall: May Contain Peanut Butter Crackers Products: RITZ CHEESE CRACKER SANDWICHES FAMILY SIZE 21.6 ounces (04400003826) Sell by codes: 18SEP20, 20SEP20, 28SEP20, 29SEP20, 30SEP20, 01OCT20, 02OCT20. 1 Some of the previous recalls … The Food and Drug Administration announced Wednesday that it will expand its recall of blood pressure medicines to include four lots of losartan … Site by Manon Etc. The FDA recently recalled blood pressure drug irbesartan for the same defect. The Sandoz Inc. recall involved 100 milligram/25 milligram Losartan tablets with the lot number JB8912 and expiration date of June 2020. BENEFIBER PREBIOTIC FIBER SUPPLEMENT. Losartan is used to treat high blood pressure (hypertension). Alembic has losartan on back order due to manufacturing delays. I can only hope…, Every school district needs positive advertising for para positions, great topic! Added April 29, 2020 Reason for recall: May … UPDATE - Teva expands its voluntary recall of losartan Update [6/12/2019] Teva Pharmaceuticals is expanding its voluntary recall to include seven additional lots of losartan potassium tablets (three lots … We'll assume you're ok with this, but you can opt-out if you wish. Patients should contact their pharmacist or physician who can advise them about an alternative treatment prior to returning their medication. Sandoz Inc. is voluntarily recalling one lot of Losartan Potassium Hydrochlorothiazide Tablets, USP 100mg/25mg to the consumer level. OTTAWA – Health Canada is advising Canadians that multiple lots of Losartan-containing … This is not the first recall of blood pressure medication for similar reasons. That product callback followed on another NDEA-related drug recall, for another blood pressure medication, valsartan,  in July. Losartan may … 12/23/2020. It's all about unity and bipartisanship until they are in charge. FDA recall on Losartan, a popular blood pressure medication. This new recall expansion is the fifth in 2019 for Torrent’s losartan products, following the initial recall on December 20, 2018. FDA does not endorse either the product or the company. We wanted to let you know that certain manufacturers have issued a recall of select lots of Losartan Potassium 100mg Tablets. According to the recall, the tainted product was distributed after Oct. 8, 2018. OTTAWA – Health Canada is advising Canadians that multiple lots of Losartan-containing drugs are being voluntarily recalled by Teva Canada, Apotex Inc., Pharmascience Inc., and Pro Doc Limitée because of the potential for a nitrosamine impurity, N-Nitroso-N-methyl-4-aminobutyric acid (NMBA). The company added five lots of the generic drug losartan (three lots of losartan potassium tablets and two lots of losartan potassium/hydrochlorothiazide tablets) to an April recall … Torrent Pharmaceuticals Ltd. has expanded its recall of losartan potassium and losartan … WASHINGTON, D.C. – The U.S. Food and Drug Administration has issued a recall on a popular blood pressure medication, citing that a “bad batch” may include a carcinogen. Now, almost a year later, manufacturer Torrent Pharmaceuticals expands its voluntary recall for the 5th time. They are centrists. UPDATE: December 2, 2020 12-2-2020 A surveillance video of the incident was sent to Texoma's Homepage by a viewer. It may be used alone or in combination with other antihypertensive agents. These cookies do not store any personal information. A recall of common blood pressure medication losartan has been expanded for a fifth time after manufacturer Torrent Pharmaceuticals found a possibly carcinogenic impurity in more … Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. The recall of Losartan is linked to a possible cancer-causing element known as NMBA. This time, the recall affects 5 lots: 3 lots of losartan potassium tablets and 2 … Share By: Nancy Clanton, The Atlanta Journal-Constitution Updated: September … He doesn't represent anything…. Losartan Potassium Tablet and Losartan Potassium/ Hydrochlorothiazide Tablet Lots. Out of these cookies, the cookies that are categorized as necessary are stored on your browser as they are essential for the working of basic functionalities of the website. En español | Torrent Pharmaceuticals announced that it has expanded its voluntary recall of blood pressure medications after testing revealed trace amounts of a known probable human carcinogen.. Withdrawals, & ... 2020 I Losartan Pot/HCTZ 50/12.5 mg 06191904090 CGMP Deviations If you have questions about this recall… The issue lies solely with the contamination. To date, Sandoz Inc. has not received any reports of adverse events related to this lot. The recall of Torrent's Losartan … Recall of metformin hydrochloride extended-release tablets 500 mg by Apotex due to N-Nitrosodimethylamine (NDMA).... Read More EDUCATION May 28, 2020 … 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. 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. Available Products Diovan oral tablet, Novartis, 160 mg, bottle, 90 count, NDC 00078-0359-34 This is an archived article and the information in the article may be outdated. Sep 18, 2020 | Updated: 09:30 AM EDT … Any cookies that may not be particularly necessary for the website to function and is used specifically to collect user personal data via analytics, ads, other embedded contents are termed as non-necessary cookies. Losartan Recall FAQs Is Losartan Safe? … We also use third-party cookies that help us analyze and understand how you use this website. ... gin May 12, 2020 at 1:38 pm … Available Products Diovan oral tablet, Novartis, 160 mg, bottle, 90 count, NDC 00078-0359-34 The Valsartan Recall List. Then we…, her mom is a denial her daughter was clearly the mastermind of this murder and everyone knows it accept for…, maybe you should try harder.....easy to blame everything on the virus which I think you are doing...sorry....think there's alot more…, In 2 years, Pappas will be gone, back cooking the chicken fingers where he belongs .. In November, the FDA announced a voluntary recall of losartan potassium/hydrochlorothiazide, 100 mg/25 mg tablets in 1,000-count plastic bottles, NDC 0781-5207 … The .gov means it’s official.Federal government websites often end in .gov or .mil. Car stolen from South Willow Street found 12 hours later after several sightings, thief at large, Weather: Bundle up this weekend for the coldest days of winter so far, Marking Time: Roadside Markers in New Hampshire’s Lakes Region, Part 2, Planning Board to hear request to change property use from equipment rental to used car dealership, Biden’s New Hampshire connection remains nearly 30 years later, Feb. 2 & Feb. 5: Landlords, property managers invited for info session on housing programs, Jan. 16-24 food and neccessities drive: Community Catalysts collecting items for those in need, Feb. 7-March 14 Tea Talks, Claiming Our Place: Blacks in ‘White Spaces’, Feb 19: Join in with AARP and the City Library for Taxes 101, Jan. 31 panel discussion: ‘Shared Legacies: The Affrican-American Jewish Civil Rights Alliance’. The makers of numerous batches of recalled generic losartan face a class action lawsuit, which says that contaminated versions of the hypertension drug sold … In general, losartan is a safe drug. Cancer. This recall is being made with the knowledge of the Food and Drug Administration. If you take blood pressure medicine, you'll want to double-check your bottle. The Recall is expanded to include an additional 36 lots of Losartan potassium Tablets USP and 68 lots of Losartan Potassium/Hydrochlorothiazide Tablets, USP. Sandoz Inc. is notifying its distributors by letter via overnight mail and patients by this public notification. Added May 2, 2020 Reason for recall: May Contain Peanut Butter Crackers Products: RITZ CHEESE CRACKER SANDWICHES FAMILY SIZE 21.6 ounces (04400003826) Sell by codes: 18SEP20, 20SEP20, 28SEP20, 29SEP20, 30SEP20, 01OCT20, 02OCT20. Click here to join the growing list of InkLink Community Ad Partners who, like us, are mission driven and believe in building community. This website uses cookies to improve your experience. 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. Torrent Pharmaceuticals Limited is expanding its recall for Losartan Potassium Tablets USP and Losartan Potassium/hydrochlorothiazide tablets, USP, to the consumer level due to the detection of trace amounts of an unexpected impurity found in an active pharmaceutical ingredient (API) manufactured by Hetero Labs Limited. 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. Class 2 Recall: Using the drug may cause temporary or medical reversible adverse health consequences, the probability of serious adverse health consequences is remote. Patients who are taking Losartan Potassium Tablets, USP and Losartan Potassium/Hydrochlorothiazide Tablets, USP should continue taking their medication, as the risk of harm to the patient’s health may be higher if the treatment is stopped immediately without any alternative treatment. The announcement  issued Nov. 8 is posted on the FDA website, describes the voluntary recall on behalf of the manufacturer, Sandoz Inc. As with previous recalls, the FDA cautions that if you take these hypertension medications, it is important to consult a pharmacist or physician before discontinuing use of the drug, as that may have even more severe effects than taking a contaminated pill. The recall involves both losartan potassium/hydrochlorothiazide tablets and losartan potassium tablets. Recalls, Market Withdrawals, & Safety Alerts, Recalls, Market Withdrawals and Safety Alerts, Recalls, Market Withdrawals, & Safety Alerts, Archive for Recalls, Market Withdrawals & Safety Alerts, Updated: Torrent Pharmaceuticals Limited Expands Voluntary Nationwide Recall of Losartan Potassium Tablets, USP and Losartan Potassium/Hydrochlorothiazide Tablets, USP, Recent Recalled Product Photos on FDA's Flickr Photostream, Losartan Potassium Tablets, USP 25mg, 90 count, Losartan Potassium Tablets, USP 25mg, 1000 count, Losartan Potassium Tablets, USP 50mg, 30 count, Losartan Potassium Tablets, USP 50mg, 90 count, Losartan Potassium Tablets, USP 50mg, 1000 count, Losartan Potassium Tablets, USP 100mg, 90 count, Losartan Potassium Tablets, USP 100mg, 1000 count, Losartan Potassium/ Hydrochlorothiazide Tablets, USP 50mg/12.5mg, 30 count, Losartan Potassium /Hydrochlorothiazide Tablets, USP 50mg/12.5mg, 90 count, Losartan Potassium/ Hydrochlorothiazide Tablets, USP 50mg/12.5mg, 90 count, Losartan Potassium / Hydrochlorothiazide Tablets, USP 50mg/12.5mg, 90 count, Losartan Potassium/ Hydrochlorothiazide Tablets, USP 50mg/12.5mg, 1000 count, Losartan Potassium/ Hydrochlorothiazide Tablets, USP 100mg/12.5mg, 30 count, Losartan Potassium/ Hydrochlorothiazide Tablets, USP 100mg/12.5mg, 90 count, Losartan Potassium/ Hydrochlorothiazide Tablets, USP 100mg/25mg, 30 count, Losartan Potassium/ Hydrochlorothiazide Tablets, USP 100mg/25mg, 90 count, Losartan Potassium/ Hydrochlorothiazide Tablets, USP 100mg/25mg, 90count, Losartan Potassium/ Hydrochlorothiazide Tablets, USP 100mg/25mg, 1000 count, Losartan Potassium/Hydrochlorothiazide Tablets, USP 100mg/25mg, 1000 count, Losartan Potassium Tablets, USP 50mg,90 count, Losartan Potassium /Hydrochlorothiazide Tablets, USP 100mg/12.5mg, 1000 count. Thanks for sharing Pop’s beautiful work and the stories that they tell. The product can be identified by checking the product name, manufacturer details and batch or lot number on the bottle containing these products. NDC 13668-409-10, losartan potassium tablets, USP 50 mg, 1,000 count, batch number 4DU2E009, expires on 12/31/2020; NDC 13668-115-90, losartan potassium tablets, USP 100 mg, 90 … It is also used to lower the risk of stroke in certain people with heart disease. Losartan is a popular blood pressure medication that has been voluntarily recalled multiple times due to the presence of a human carcinogen. WASHINGTON – The Food and Drug Administration has again expanded a recall for medication used to treat high blood pressure over contamination with a chemical linked to cancer. The Sandoz Inc. recall involved 100 milligram/25 milligram Losartan tablets with the lot number JB8912 and expiration date of June 2020. Losartan is used to treat hypertension, hypertensive patients with Left Ventricular Hypertrophy and for the treatment of nephropathy in Type 2 diabetic patients. 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. Another recall on Losartan has been announced due to the reported carcinogenic substances contained in the blood pressure medication. Consumers should also contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. This is linked to an impurity in those medications, called NDMA. Some viewers may find the content graphic and/or violent. The recall did not include all batches (also called lots) of these … Losartan is used to slow long-term kidney damage in people with type 2 diabetes who also have high blood pressure. Yes -- the safety of the drug itself is not the issue in the recall of losartan. BENEFIBER PREBIOTIC FIBER SUPPLEMENT. When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. 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. Any general questions regarding the return of this product should be directed to Qualanex at 1- 888-280-2040 (live calls received 8 am - 9:00 pm Eastern Time). Torrent Pharmaceuticals Limited is expanding its recall for Losartan Potassium Tablets USP and Losartan Potassium/hydrochlorothiazide tablets, USP, to the consumer level due to the detection … The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. The recall included both losartan potassium tablets USP and combination tablets containing both losartan and hydrochlorothiazide. Patients should contact their pharmacist or physician who can advise them about an alternative treatment prior to returning their medication. You also have the option to opt-out of these cookies. Once Upon a Pie Baking Competition & Auction. This product was distributed nationwide to distributors. The impurity detected in the API is N-Methylnitrosobutyric acid (NMBA). Complete and submit the report Online: www.fda.gov/medwatch/report.htm, Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm, Call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178, More Recalls, Market The affected lots are being recalled due to an unexpected … Losartan is … The actual Left does n't like Obama or Biden either experience unexpected weight gain but opting of! The Pop ’ s Art section be linked to liver cancer, colorectal cancer, colorectal cancer, cancer... We 'll assume you 're on a federal government site behalf of the Food drug! Federal government site combination with other antihypertensive agents browser only with your consent website, describes voluntary!, January 22, March 1, and kidney cancer overnight mail and by... Recently recalled blood pressure medication contact their pharmacist or physician who can advise them about an treatment! 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