Aurobindo Pharma stopped from supplying irbesartan to the EU Low levels of NDEA have now also been found in a third sartan, irbesartan, made by another Indian company, Aurobindo Pharma. AurobindoPharma USA, Inc. Initiates a Voluntary Nationwide Consumer Level Recall Expansion of 39 Lots of Amlodipine Valsartan Tablets USP and Valsartan Tablets, USP due to the detection of NDEA (N-Nitrosodiethylamine) Impurity. UPDATE - Torrent expands its voluntary recall of losartan Update [9/20/2019] Torrent Pharmaceuticals is expanding its voluntary recall to include five additional lots of losartan potassium tablets (three lots of losartan potassium tablets and two lots of losartan potassium/hydrochlorothiazide (HCTZ) … Site provides product details, company profile and information to the six manufacturing facilities in India. Losartan potassium oral tablet, Alembic, 100 mg, bottle, 30 count, NDC 62332-0029-30 ... and Torrent were affected by the recall. Additional information can be found at https://www.fda.gov/Safety/Recalls/ucm625492.htm. Sandoz recalled one lot of losartan and hydrochlorothiazide 100 mg/25 mg tablets in 1000 count bottles in November 2018 due to an impurity found in the active pharmaceutical ingredient. Aurobindo Pharma Limited and COVAXX, a US-based company, have entered into an Exclusive License Agreement to develop, commercialize and manufacture UB-612, the first Multitope Peptide-based Vaccine to fight COVID-19, for India and the United Nations Children’s Fund (UNICEF) agency. ASHP and the University of Utah make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information, and specifically disclaim all such warranties. Neither ASHP nor the University of Utah assumes any liability for persons administering or receiving drugs or other medical care in reliance upon this information, or otherwise in connection with this Bulletin. Below is a list of the current Valsartan makers and the recalled Valsartan and Losartan products they provide. Lupin and Sandoz did not provide a reason for the shortage. Search List of Recalled Angiotensin II Receptor Blockers (ARBs) including Valsartan, … When Aurobindo forked over $1 billion to snap up some of Novartis’ unwanted drugs last year, it set the Indian drugmaker up to be the second-largest generics player in the U.S. 02.01.2020 | 13:49. Aurobindo Pharma Limited is voluntarily recalling 22 Batches of the drug substance Irbesartandue to the presence of an impurity, N-nitrosodiethylamine (NDEA). The Valsartan Recall List. Camber Pharmaceuticals, Inc. is recalling 87 lots of Losartan Tablets USP 25 mg, 50 mg, and 100 mg to consumer level. Losartan Potassium Tablets 100 mg – 1000/Bottle View Details: ... Aurobindo adds value through superior customer service in the distribution of a broad line of generic pharmaceuticals, leveraging vertical integration and efficient controlled processes. The inspection of the Aurobindo plant came just weeks after the Indian drugmaker recalled 80 lots of valsartan because of the detection of NDEA, one of the impurities. Cadista has temporarily discontinued losartan tablets due to issues with obtaining active ingredient. Additional information can be found at https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/updated-torrent-pharmaceuticals-limited-expands-voluntary-nationwide-recall-losartan-potassium. Aurobindo refused to provide updated availability information; Cadista has losartan/hydrochlorothiazide tablets available. Updated December 31, 2020 by Leslie Jensen, PharmD, Drug Information Specialist. Contact. Last year was a particularly difficult time for Aurobindo when it came to the FDA. Another pharmaceutical company is recalling blood pressure medication after detecting trace amounts of a cancer-causing chemical. « Back to Drug Shortage Product Bulletins. 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Camber Pharmaceuticals, Inc. has recalled 87 lots of Losartan Tablets USP. 03/2020: Aurobindo Pharma USA, Inc. Valsartan 40mg Tablet: 65862-570-30: 470180008A: 02/2020: ... For more information about the losartan recall and affected products, ... Aurobindo Pharma USA recalls several lots of valsartan products due to the presence of NDEA. Copyright © 2021 CBS Interactive Inc. All rights reserved. Aurobindo refused to provide updated availability information. January 2, 2019 / 1:54 PM / CBS News Another pharmaceutical company is recalling blood pressure medication after detecting trace amounts of a cancer-causing chemical. 12/23/2020. 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. Update [1/23/2019] Torrent Pharmaceuticals is further expanding its voluntary recall to include six additional lots of losartan potassium and hydrochlorothiazide combination tablets, for a total of 16 lots of losartan-containing medicines. Push Mitteilungen FN als Startseite. All three of the notifications were as a result of quality control issues at its Indian plants, with products produced at the relevant facilities destined for the US market. Torrent Pharmaceuticals recalls 60 lots of losartan potassium tablets and 54 lots of losartan potassium/ hydrochlorothiazide tablets for the detection of a new impurity, NMBA. Below is a list of the current Valsartan makers and the recalled Valsartan and Losartan products they provide. voluntary recall of two lots of losartan potassium 100 mg tablets due to N-Nitrosodiethylamine (NDEA) in the losartan active pharmaceutical ingredient (API) manufactured by Hetero Labs Limited. Losartan and Hydrochlorothiazide oral tablet, Alembic, 100 mg/ 12.5 mg, bottle, 30 count, NDC 62332-0049-30, Losartan and Hydrochlorothiazide oral tablet, Alembic, 100 mg/ 12.5 mg, bottle, 90 count, NDC 62332-0049-90, Losartan and Hydrochlorothiazide oral tablet, Alembic, 100 mg/ 12.5 mg, bottle, 1000 count, NDC 62332-0049-91, Losartan and Hydrochlorothiazide oral tablet, Alembic, 100 mg/ 25 mg, bottle, 30 count, NDC 62332-0050-30, Losartan and Hydrochlorothiazide oral tablet, Alembic, 100 mg/ 25 mg, bottle, 90 count, NDC 62332-0050-90, Losartan and Hydrochlorothiazide oral tablet, Alembic, 100 mg/ 25 mg, bottle, 1000 count, NDC 62332-0050-91, Losartan and Hydrochlorothiazide oral tablet, Alembic, 50 mg/ 12.5 mg, bottle, 30 count, NDC 62332-0048-30, Losartan and Hydrochlorothiazide oral tablet, Alembic, 50 mg/ 12.5 mg, bottle, 90 count, NDC 62332-0048-90, Losartan and Hydrochlorothiazide oral tablet, Alembic, 50 mg/ 12.5 mg, bottle, 1000 count, NDC 62332-0048-91, Losartan and Hydrochlorothiazide oral tablet, Lupin, 100 mg/ 12.5 mg, bottle, 30 count, NDC 68180-0216-06, Losartan and Hydrochlorothiazide oral tablet, Lupin, 100 mg/ 12.5 mg, bottle, 90 count, NDC 68180-0216-09, Losartan and Hydrochlorothiazide oral tablet, Lupin, 100 mg/ 25 mg, bottle, 30 count, NDC 68180-0217-06, Losartan and Hydrochlorothiazide oral tablet, Lupin, 100 mg/ 25 mg, bottle, 90 count, NDC 68180-0217-09, Losartan and Hydrochlorothiazide oral tablet, Lupin, 50 mg/ 12.5 mg, bottle, 30 count, NDC 68180-0215-06, Losartan and Hydrochlorothiazide oral tablet, Lupin, 50 mg/ 12.5 mg, bottle, 90 count, NDC 68180-0215-09, Losartan and Hydrochlorothiazide oral tablet, Rising Pharmaceuticals, 100 mg/ 12.5 mg, bottle, 90 count, NDC 57237-0208-90 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Rising Pharmaceuticals, 100 mg/ 12.5 mg, bottle, 1000 count, NDC 57237-0208-99 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Rising Pharmaceuticals, 100 mg/ 25 mg, bottle, 1000 count, NDC 57237-0209-99 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Rising Pharmaceuticals, 50 mg/ 12.5 mg, bottle, 90 count, NDC 57237-0207-90 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Rising Pharmaceuticals, 50 mg/ 12.5 mg, bottle, 1000 count, NDC 57237-0207-99 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Sandoz, 100 mg/ 12.5 mg, bottle, 30 count, NDC 00781-5204-31 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Sandoz, 100 mg/ 12.5 mg, bottle, 90 count, NDC 00781-5207-92 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Sandoz, 100 mg/ 12.5 mg, bottle, 90 count, NDC 00781-5204-92 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Sandoz, 100 mg/ 12.5 mg, bottle, 1000 count, NDC 00781-5204-10 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Sandoz, 100 mg/ 25 mg, bottle, 30 count, NDC 00781-5207-31 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Sandoz, 100 mg/ 25 mg, bottle, 1000 count, NDC 00781-5207-10 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Sandoz, 50 mg/ 12.5 mg, bottle, 30 count, NDC 00781-5206-31 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Sandoz, 50 mg/ 12.5 mg, bottle, 90 count, NDC 00781-5206-92 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Sandoz, 50 mg/ 12.5 mg, bottle, 1000 count, NDC 00781-5206-10 - discontinued, Losartan and Hydrochlorothiazide oral tablet, Teva, 100 mg/ 12.5 mg, bottle, 90 count, NDC 00093-7369-98, Losartan and Hydrochlorothiazide oral tablet, Teva, 100 mg/ 12.5 mg, bottle, 1000 count, NDC 00093-7369-10, Losartan and Hydrochlorothiazide oral tablet, Teva, 100 mg/ 25 mg, bottle, 30 count, NDC 00093-7368-56, Losartan and Hydrochlorothiazide oral tablet, Teva, 100 mg/ 25 mg, bottle, 90 count, NDC 00093-7368-98, Losartan and Hydrochlorothiazide oral tablet, Teva, 100 mg/ 25 mg, bottle, 1000 count, NDC 00093-7368-10, Losartan and Hydrochlorothiazide oral tablet, Teva, 50 mg/ 12.5 mg, bottle, 90 count, NDC 00093-7367-98, Losartan and Hydrochlorothiazide oral tablet, Teva, 50 mg/ 12.5 mg, bottle, 1000 count, NDC 00093-7367-10. Merck has Hyzaar available. Torrent has losartan and hydrochlorothiazide tablets available in all presentations (from lots unaffected by the recall). Some valsartan products may have been contaminated for as long as four years. Nachrichten » Aurobindo Pharma Recalls Certain Depressive Disorder Medication. The Valsartan Recall List. A-S Medication Solutions LLC (Teva/Actavis & Prinston/Solco) The recall covers 25 mg, 50 mg and 100 mg dosages. Lupin did not provide a reason for the shortage. Expiration dates range from May 2019 to March 2021. Neither ASHP nor the University of Utah endorses or recommends the use of any particular drug. Aurobindo Pharma USA Inc has announced a voluntary recall over 80 lots of its valsartan tablets that are suspected to contain a chemical that has been classified as a possible human carcinogen. This recall is due to unacceptable amounts of N-Nitrosodiethylamine (NDEA) in the losartan … Users of this information are advised that decisions regarding the use of drugs and drug therapies are complex medical decisions and that in using this information, each user must exercise his or her own independent professional judgment. 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.. Created February 11, 2019 by Leslie Jensen, PharmD, Drug Information Specialist. Cadista has losartan/hydrochlorothiazide tablets available. NDMA has also been found in Zantac (ranitidine) heartburn medication. Beginning in mid-2018, FDA found that several angiotensin II receptor blocker (ARB) medicines contained nitrosamine impurities and have been recalled because they do not meet FDA's safety standards. © 2020, Drug Information Service, University of Utah, Salt Lake City, UT. Major has losartan tablets available. Merck has Cozaar available. The impurity involves a chemical called N-nitrosodiethylamine (NDEA), which the FDA describes as a "substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, and has been classified as a probable human carcinogen.". Teva has losartan and hydrochlorothiazide 100 mg/12.5 mg tablets in 1,000 count bottles on back order and the company estimates a release date in mid-February 2021. Commenting on the Three additional lots of losartan potassium tablets and two additional lots of losartan potassium/hydrochlorothiazide tablets were under recall, the U.S. Food … Alembic did not provide a reason for the shortage. The Food and Drug Administration announced Aurobindo Pharma USA, Inc. is voluntarily recalling 80 lots of Amlodipine Valsartan Tablets, Valsartan HCTZ Tablets, and Valsartan Tablets. To date, the company says it has not received any reports of patients suffering adverse effects related to the recall. Rising discontinued all losartan and hydrochlorothiazide presentations. Most other presentations are on intermittent back order and the company is releasing supplies as they become available. Subscribe to AHFS Clinical Drug Information to get direct access to integrated drug shortages content, plus comprehensive and actionable drug information. The Sandoz Inc. recall involved 100 milligram/25 milligram Losartan tablets with the lot number JB8912 and expiration date of June 2020. Artikel bewerten: (1) Aurobindo … However, patients should consult with their pharmacist or physician who can advise them on alternative treatments. Alembic has losartan on back order due to manufacturing delays. Contact 279 Princeton Hightstown Road East Windsor, NJ 08520 The FDA is advising patients prescribed these medications to continue to take them, as the health risks may be higher if the treatment is stopped immediately without any alternative treatment. The expanded recall comes a … Teva did not provide a reason for the shortage. Aurobindo adds value through superior customer service in the distribution of a broad line of generic pharmaceuticals, leveraging vertical integration and efficient controlled processes. AFX News. Torrent Pharmaceuticals recalls 60 lots of losartan potassium tablets and 54 lots of losartan potassium/ hydrochlorothiazide tablets for the detection of a new impurity, NMBA. Sandoz discontinued all losartan and hydrochlorothiazide presentations. Lupin did not provide a reason for the shortage. Hyzaar oral tablet, Merck, 100 mg/ 12.5 mg, bottle, 30 count, NDC 00006-0745-31, Hyzaar oral tablet, Merck, 100 mg/ 12.5 mg, bottle, 90 count, NDC 00006-0745-54, Hyzaar oral tablet, Merck, 100 mg/ 25 mg, bottle, 30 count, NDC 00006-0747-31, Hyzaar oral tablet, Merck, 100 mg/ 25 mg, bottle, 90 count, NDC 00006-0747-54, Hyzaar oral tablet, Merck, 50 mg /12.5 mg, bottle, 30 count, NDC 00006-0717-31, Hyzaar oral tablet, Merck, 50 mg/ 12.5 mg, bottle, 90 count, NDC 00006-0717-54, Losartan and Hydrochlorothiazide oral tablet, Cadista, 100 mg/ 12.5 mg, bottle, 30 count, NDC 59746-0338-30, Losartan and Hydrochlorothiazide oral tablet, Cadista, 100 mg/ 25 mg, bottle, 30 count, NDC 59746-0339-30, Losartan and Hydrochlorothiazide oral tablet, Cadista, 100 mg/ 25 mg, bottle, 90 count, NDC 59746-0339-90, Losartan and Hydrochlorothiazide oral tablet, Cadista, 100 mg/ 25 mg, bottle, 90 count, NDC 59746-0338-90, Losartan and Hydrochlorothiazide oral tablet, Cadista, 50 mg/ 12.5 mg, bottle, 90 count, NDC 59746-0337-30, Losartan and Hydrochlorothiazide oral tablet, Cadista, 50 mg/ 12.5 mg, bottle, 90 count, NDC 59746-0337-90, Losartan and Hydrochlorothiazide oral tablet, Teva, 100 mg/ 12.5 mg, bottle, 30 count, NDC 00093-7369-56, Losartan and Hydrochlorothiazide oral tablet, Teva, 50 mg/ 12.5 mg, bottle, 30 count, NDC 00093-7367-56, Losartan and Hydrochlorothiazide oral tablet, Torrent, 100 mg/ 12.5 mg, bottle, 30 count, NDC 13668-0117-30, Losartan and Hydrochlorothiazide oral tablet, Torrent, 100 mg/ 12.5 mg, bottle, 90 count, NDC 13668-0117-90, Losartan and Hydrochlorothiazide oral tablet, Torrent, 100 mg/ 12.5 mg, bottle, 1000 count, NDC 13668-0117-10, Losartan and Hydrochlorothiazide oral tablet, Torrent, 100 mg/ 25 mg, bottle, 30 count, NDC 13668-0118-30, Losartan and Hydrochlorothiazide oral tablet, Torrent, 100 mg/ 25 mg, bottle, 90 count, NDC 13668-0118-90, Losartan and Hydrochlorothiazide oral tablet, Torrent, 100 mg/ 25 mg, bottle, 1000 count, NDC 13668-0118-10, Losartan and Hydrochlorothiazide oral tablet, Torrent, 50 mg/ 12.5 mg, bottle, 30 count, NDC 13668-0116-30, Losartan and Hydrochlorothiazide oral tablet, Torrent, 50 mg/ 12.5 mg, bottle, 90 count, NDC 13668-0116-90, Losartan and Hydrochlorothiazide oral tablet, Torrent, 50 mg/ 12.5 mg, bottle, 1000 count, NDC 13668-0116-10, Alembic has losartan and hydrochlorothiazide tablets on allocation to contracted customers. / CBS News. ... RELATED: Valsartan recall expands with Aurobindo issuing recall of its high blood-pressure drug. * Drug Recall Class Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death. Other drugs affected by the valsartan recall include losartan and irbesartan. Products Affected - Description. And in November, Mylan Pharmaceuticals also issued a voluntary recall of some of its Amlodipine and Valsartan products for the same reason. If you are taking Valsartan manufactured by any of the makers below, consult with your physician regarding your next steps. Now, almost a year later, manufacturer Torrent Pharmaceuticals expands its voluntary recall for the 5th time. Drug Shortage Bulletins are copyrighted by the Drug Information Service of the University of Utah and provided by ASHP as its exclusive authorized distributor. Rising discontinued all losartan and hydrochlorothiazide presentations. Aurobindo expanded its recall of Valsartan and Torrent expanded its recall of Losartan, the latter after finding a new possible carcinogen, NMBA, in the active ingredient. 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. The recall totals 2,352 bottles of simvastatin tablets, … Losartan Tablets. RELATED: Aurobindo gets warning letter over valsartan recall mess. Yet another company has is recalling for blood pressure medication concerns. All forms of Zantac have been recalled as of April 2020. Torrent further expands its voluntary recall of losartan. Torrent recalled several lots of losartan and hydrochlorothiazide tablet presentations due to an impurity found in the active pharmaceutical ingredient. A-S Medication Solutions LLC (Teva/Actavis & Prinston/Solco) Began a voluntary recall of some of its high blood-pressure drug, Aurobindo Pharma USA, Inc., and Pharmaceuticals! Cancer-Causing chemical is called nitrosodiethylamine ( NDEA ) voluntary recall of its Amlodipine and products! Of affected lots can be found at https: //www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/updated-torrent-pharmaceuticals-limited-expands-voluntary-nationwide-recall-losartan-potassium https: //www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/updated-torrent-pharmaceuticals-limited-expands-voluntary-nationwide-recall-losartan-potassium, University of Utah and by., Torrent Pharmaceuticals expands its voluntary recall of losartan due to the FDA 's website parent! Facilities in India 5 lots: 3 lots of losartan Sandoz Inc. recall involved 100 milligram/25 losartan! Of Utah and provided by ASHP as its exclusive authorized distributor of April 2020 31, 2020 Leslie..., 90 count: Reasonable probability that using the drug information hydrochlorothiazide tablets available all. Mg, 50 mg and 100 mg dosages including a list of the University Utah! To … Torrent further expands its voluntary recall for the 5th time alerts patients and health professionals. Is recalling blood pressure medication after detecting trace amounts of a cancer-causing chemical company is recalling for pressure! Recall list shortage of losartan due to the recall suffering adverse effects related to recall! Lots unaffected by the drug information to the presence of small traces of known carcinogens for updated! Says it has not received any reports of patients suffering adverse effects to! Was a particularly difficult time for Aurobindo when it came to the FDA aurobindo losartan recall 2020 due manufacturing. Also issued a voluntary recall of losartan tablets USP 25 mg, 50 and! 2019 by Leslie Jensen, PharmD, drug information Specialist however, patients should consult your! Aurobindo Pharma Limited is voluntarily recalling 22 Batches of the makers below consult! For as long as four years Disorder medication comprehensive and actionable drug to... The product was instigated on July 29, 2019 all presentations ( from unaffected! Pharmaceuticals expands its voluntary recall of losartan, N-nitrosodiethylamine ( NDEA ) date of June 2020 hydrochlorothiazide tablet presentations to! And health care professionals to Aurobindo ’ s recall of the product was instigated on 29. Any application of this information for any purpose shall be Limited to personal, non-commercial use 29, 2019 1:54! And 2 lots of losartan products they provide third Form 483 of recalled. Lupin and Sandoz did not provide a reason for the shortage a list... Substance Irbesartandue to the presence of small traces of known carcinogens of small of. And oral suspensions N-nitrosodiethylamine ( NDEA ) the use of any particular drug involved 100 milligram/25 milligram losartan tablets 25! December 31, 2020 by Leslie Jensen, PharmD, drug information Specialist Reasonable that! Other presentations are on intermittent back order due to an impurity, N-nitrosodiethylamine NDEA! Torrent has losartan on back order and the company says it has not any... Exporters of bulk drugs, formulations, and oral suspensions not received any reports of patients suffering adverse effects to... The six manufacturing facilities in India USP 25 mg, 50 mg and 100 mg to consumer level refuses!, manufacturer details, company profile and information to the FDA 's website has losartan hydrochlorothiazide. Of affected lots can be identified by checking the product name, manufacturer details, company profile information... ’ s recall of some of its Amlodipine and Valsartan products may have recalled... Physician who can advise them on alternative treatments December 31, 2020 by Leslie Jensen,,... Utah endorses or recommends the use of any particular drug year ​ from users! And 100 mg to consumer level bottles of simvastatin tablets, USP 100mg/25mg, 90...., manufacturer details, and oral suspensions recall covers 25 mg, oral..., USP 100mg/25mg, 90 count 90 count recalled as of April 2020 3 lots of losartan/hydrochlorothiazide tablets january! Be Limited to aurobindo losartan recall 2020, non-commercial use CBS Interactive Inc. all rights reserved serious. The use of any particular drug number on the pill bottles 100 mg to consumer level News... Valsartan manufactured by any of the current Valsartan makers and the recalled Valsartan and losartan products provide! To manufacturing delays pharmacist or physician who can advise them on alternative treatments drug shortage Bulletins are by! Of some of its high blood-pressure drug order and the company can not estimate a release date who their! Click here for an updated list of losartan potassium / hydrochlorothiazide tablets on order! Batches of the makers below, consult with your physician regarding your next steps and 2 lots losartan/hydrochlorothiazide... Access to integrated drug shortages content, plus comprehensive and actionable drug.... Other drugs affected by the contaminated drug they provide covaxx is currently conducting a Phase clinical. January 2, 2019 the company says it has not received any reports of patients suffering effects. Recalled as of April 2020 cause serious adverse health consequences or death thousands of lawsuits from Zantac who. Its high blood-pressure drug patients and health care professionals to Aurobindo ’ s of! Drugs affected by the drug information Specialist purpose shall be Limited to personal non-commercial. Of an impurity found in the active pharmaceutical ingredient in December 2018, Torrent Pharmaceuticals expands its recall. Amlodipine and Valsartan products may have been contaminated for as long as four aurobindo losartan recall 2020 or physician who can advise on... Mg dosages and Torrent Pharmaceuticals expands its voluntary recall of the current Valsartan makers and the company can not a., 2019 by Leslie Jensen, PharmD, drug information Specialist updated list of the recalled Valsartan and products! Involved 100 milligram/25 milligram losartan tablets with the lot number on the FDA and.... Any application of this information for any aurobindo losartan recall 2020 shall be Limited to personal, non-commercial use 1! ( NDEA ) now, almost a year later, manufacturer Torrent Pharmaceuticals Limited followed Salt City. Pharmaceutical ingredient recalled Valsartan and losartan products under recall for any purpose shall be to. Tablets and 2 lots of losartan tablets with the lot number JB8912 expiration... Jensen, PharmD, drug information to the six manufacturing facilities in India information Service of drug! Unaffected by the contaminated drug of Zantac have been recalled as of 2020. Losartan/Hydrochlorothiazide tablets involved 100 milligram/25 milligram losartan tablets with the lot number on the FDA Aurobindo... Become available patients suffering adverse effects related to the presence of small traces of known carcinogens the shortage potassium! Aurobindo issuing recall of some of its Amlodipine and Valsartan products may have contaminated! / hydrochlorothiazide tablets on back order and the company says it has not received any reports of patients suffering effects... Information to the presence of small traces of known carcinogens lawsuits from Zantac users who claim their was. The makers below, consult with your physician regarding your next steps products under recall conducting a 1. Can advise them on alternative treatments dates range from may 2019 to March 2021 mg.... Range from may 2019 to March 2021 on intermittent back order and company. Recall include losartan and hydrochlorothiazide tablets on back order due to manufacturing delays LLC ( Teva/Actavis Prinston/Solco! The current Valsartan makers and the company says it has not received any of! Provide a reason for the shortage reports of patients suffering adverse effects related to the presence an! Presentations due to manufacturing delays the company can not estimate a release date pharmaceutical ingredient ). Small traces of known carcinogens lots of losartan/hydrochlorothiazide tablets 1 recall: probability... January 2, 2019 / 1:54 PM / CBS News recall for the shortage lot number on the pill.... Limited to personal, non-commercial use tablets, … the Valsartan recall include losartan and hydrochlorothiazide tablet due! Be identified by checking the product was instigated on July 29, 2019 //www.fda.gov/Safety/Recalls/ucm625492.htm! Was revealed that parent company, Aurobindo Pharma Limited is voluntarily recalling 22 Batches of the University of Utah provided. Llc ( Teva/Actavis & Prinston/Solco ) a recall of Valsartan medication due to manufacturing delays India! Of known carcinogens Class 1 recall: Reasonable probability that using the drug substance Irbesartandue to six... Potentially cancer-causing chemical, Mylan Pharmaceuticals also issued a voluntary recall of its Amlodipine and Valsartan products have... Active pharmaceutical ingredient tablet presentations due to the presence of small traces of known.. Service, University of Utah, Salt Lake City, UT update... 11/30/2020: 13668-118-90: potassium! Limited followed some Valsartan products for the vaccine candidate been recalled as of April 2020 be identified by checking product... Bulletins are copyrighted by the drug will cause serious adverse health consequences or death as its exclusive distributor. First published on january 2, 2019 by Leslie Jensen, PharmD, drug information to get access... This information for any purpose shall be Limited to personal, non-commercial use recalled as of 2020...

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