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DIOVAN RECALL

Massive Valsartan Voluntary FDA Recall. In July , the FDA prompted Valsartan's first voluntary recall by Teva Pharmaceuticals, labeled Major. On July 13, , the U.S. Food and Drug Administration (FDA) announced a voluntary recall of Valsartan after some was discovered to contain. Many people after taking valsartan medications like Diovan, Diovan HCT, Exforge, Exforge HCT and Entresto are horrified to learn that their medication could. In one year, the FDA recalled more than generic valsartan medications due to contamination. See if your valsartan is on the list of recalls. Valsartan is an oral medication prescribed for the treatment of high blood pressure and congestive heart failure. It was originally approved by the FDA in

In July , the FDA recalled Valsartan after studies showed that the drug In the wake of the FDA's Valsartan recall, several drug manufacturers issued. Batches of Valsartan, an angiotensin II receptor blocker known by the brand name Diovan, have been recalled due to cancer-causing impurities. One maker of Valsartan, Amlodipine/Valsartan and Valsartan/Hydrochlorothiazide is recalling certain lots of these medicines because they may have small amounts. The Valsartan recall resulted because of the presence of the potentially cancer-causing impurity, N-nitrosodimethylamine (NDMA). The FDA believes that the. These lawsuits are being brought by individuals and classes of plaintiffs based upon: economic damages from purchasing the recalled drugs; personal injury. Health Canada issued an advisory on July 9, , detailing a manufacturers' recall of products containing valsartan, due to an impurity that could have. This recall is due to an impurity, N-nitrosodimethylamine (NDMA), which was found in the recalled products. NDMA is classified as a probable human carcinogen (a. Update 05/07/ The HPRA alongside the European regulatory network are undertaking a precautionary recall of a number of specific medicines containing the. Food and Drug Administration (FDA) announces additional impurity in valsartan (Diovan®) recall. October 10, views. View Full Issue (Volume 8, Issue 1) valsartan was found in three lots of Torrent Pharmaceuticals' recalled valsartan drug products.

In March , the FDA approved a new generic of valsartan manufactured by Alkem Laboratories Ltd. to help address the valsartan and losartan shortages. The. On July 13th, the FDA announced a recall of medications containing Valsartan, a generic medication used to treat high blood pressure and heart failure from. In the summer of , several valsartan products were recalled in Canada and worldwide because of the impurity, N-nitrosodimethylamine (NDMA), found in the. The drug Valsartan used to help those with high blood pressure and heart failure was found having cancer causing carginogens and potential liver damage. Health Canada said on Tuesday July 9, , that numerous varieties of valsartan are being recalled over fears they contain the impurity NDMA, a chemical that's. There are 1, Valsartan lawsuits pending in the class action in federal court. If you have a potential Valsartan recall lawsuit, call a lawyer handling these. The primary reason for recent valsartan lawsuits is that patients were harmed by contamination that took place during the manufacture of the drugs in India and. Valsartan has been recalled because of high levels of NDMA, or N-nitrosodimethylamine. NDMA is a human carcinogen, or cancer causing substance. Valsartan and. The drug recall attorneys at McWhirter, Bellinger & Associates law firm, are reviewing potential Valsartan lawsuits. Valsartan (Diovan) is a drug prescribed.

On July 13, , the United States Food and Drug Administration announced a separate recall of valsartan from non-Sandoz companies. This recall does NOT impact. Valsartan Lawsuit The legal action, which was filed on behalf of the plaintiffs and all similarly situated consumers, accuses Solco Healthcare and Prinston. If you received recalled product from another pharmacy, please contact that pharmacy. If you are currently taking valsartan tablets and have questions regarding. The recall occurred after the company determined the presence of NDMA in the valsartan. The FDA also provided guidance to manufacturers regarding how to.

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