This recall is due to unacceptable amounts of N-Nitrosodiethylamine (NDEA) in the losartan … Camber Pharmaceuticals, Inc. is recalling 87 lots of Losartan Tablets USP 25 mg, 50 mg, and 100 mg to consumer level. Rising discontinued losartan in August 2019. 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. In June 2019, it was revealed that parent company, Aurobindo, had received its third Form 483 of the year ​. The expanded recall comes a … Created February 11, 2019 by Leslie Jensen, PharmD, Drug Information Specialist. First published on January 2, 2019 / 1:54 PM. Another pharmaceutical company is recalling blood pressure medication after detecting trace amounts of a cancer-causing chemical. Last month, Torrent Pharmaceuticals Limited issued a voluntary recall of two lots of Losartan potassium tablets over similar concerns surrounding trace amounts of NDEA. Teva did not provide a reason for the shortage. This time, the recall affects 5 lots: 3 lots of losartan potassium tablets and 2 lots of losartan/hydrochlorothiazide tablets. Cadista has temporarily discontinued losartan tablets due to issues with obtaining active ingredient. ... FDA alerts patients and health care professionals to Aurobindo’s recall of valsartan medication due to NDEA. Artikel bewerten: (1) Aurobindo … Lupin and Sandoz did not provide a reason for the shortage. The recall totals 2,352 bottles of simvastatin tablets, … Drug Shortage Bulletins are copyrighted by the Drug Information Service of the University of Utah and provided by ASHP as its exclusive authorized distributor. Products Affected - Description. However, patients should consult with their pharmacist or physician who can advise them on alternative treatments. A-S Medication Solutions LLC (Teva/Actavis & Prinston/Solco) Rising discontinued all losartan and hydrochlorothiazide presentations. 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. Site provides product details, company profile and information to the six manufacturing facilities in India. ... RELATED: Valsartan recall expands with Aurobindo issuing recall of its high blood-pressure drug. 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 … All forms of Zantac have been recalled as of April 2020. Additional information including a list of affected lots can be found at https://www.fda.gov/drugs/drug-safety-and-availability/recalls-angiotensin-ii-receptor-blockers-arbs-including-valsartan-losartan-and-irbesartan. * Drug Recall Class Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death. The Valsartan Recall List. 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