Aurobindo Valsartan Recall 2019 ::

02/01/2019 · Another company is recalling its blood pressure medication valsartan over concerns that tablets might contain trace amounts of a cancer-causing ingredient. Aurobindo Pharma USA, Inc. is voluntarily recalling 80 lots of its valsartan tablets that might include N. 01/01/2019 · Aurobindo Pharma USA is voluntarily recalling 80 lots of Amlodipine Valsartan Tablets USP, Valsartan HCTZ Tablets, USP and Valsartan Tablets USP to the consumer level, due to the detection of trace amounts N-nitrosodiethylamine NDEA. An unexpected impurity, NDEA is. Aurobindo is only recalling lots of valsartan-containing medication where NDEA has been detected above the interim acceptable intake limit of 0.083 parts per million. FDA is working with manufacturers to reduce and remove nitrosamines from angiotensin II receptor blockers ARBs. The agency also updated the valsartan products under recall. Recall of Valsartan-Containing Products by Aurobindo Effective Date: March 6, 2019 On February 25, 2019, Aurobindo announced a voluntary recall of several lots of Valsartan and Amlodipine / Valsartan tablets because of the presence of trace amounts of an unexpected impurity, N-nitrosodiethylamine NDEA, found in the finished product.

02/07/2019 · India’s Aurobindo has been one of the culprits found manufacturing the high blood pressure medicine valsartan with high levels of impurities that carry a risk of cancer. Now the FDA has savaged it in a warning letter for missteps that paved the pathway to the mess. Yet another company has is recalling for blood pressure medication concerns. 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 potentially cancer-causing chemical is called nitrosodiethylamine NDEA. They also received notification via U.S. Mail advising him that the valsartan-containing medication that they were taking was affected by the recall. It is unknown at this time how many manufacturers have produced contaminated valsartan as the list continues to grow. 02/01/2019 · Another pharmaceutical company is recalling blood pressure medication after detecting trace amounts of a cancer-causing chemical. The Food and Drug Administration announced Aurobindo Pharma USA, Inc. is voluntarily recalling 80 lots of Amlodipine Valsartan Tablets, Valsartan.

The FDA has added 80 lots of Amlodipine Valsartan blood pressure medication to the hypertension drug recall list that continues to grow. Aurobindo Pharma USA recalls lots of valsartan, amlodipine-valsartan, and valsartan-hydrochlorothiazide tablets. Aurobindo B.V. heeft in overleg met de Inspectie Gezondheidszorg en Jeugd IGJ besloten om met onmiddellijke ingang een aantal valsartan bevattende producten uit de markt terug te roepen. De aanleiding is dat in deze producten te grote hoeveelheden. 08/01/2019 · The recall of high blood-pressure drug valsartan is expanding as Indian drugmaker Aurobindo issued a voluntary recall of 80 lots of tablets of the compound due to the detection of trace amounts of an impurity found in the finished product. The recall, which was posted on.

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