5 Apr 2019 Mylan has recalled all lots of valsartan-containing products and Aurobindo In March, 2019, Aurobindo Pharma USA expanded their recall to 

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In July 2018, the FDA announced a voluntary recall of several drugs containing valsartan, used to treat high blood pressure and heart failure, because of contamination with an impurity, the potentially cancer-causing chemical N-nitrosodimethylamine, or NDMA. Other drugs affected by the valsartan recall include losartan …

The federal agency stated that the medication to treat heart failure and high blood pressure contained a toxic chemical. Valsartan Recall Lawsuit The manufacturers of Valsartan are facing lawsuits after the drug was recalled for causing injury in some patients. People visit doctors and take medication when they are trying to recover from certain medical conditions. One such drug, Valsartan, was intended to treat patients with high blood pressure and heart failure.

Valsartan recall

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Teva Pharmaceuticals voluntarily recalled two of its drugs in November over the same concerns. In August, the FDA announced an expanded recall of valsartan because products might contain the impurity. The voluntary valsartan recall specifically applies to certain valsartan and valsartan hydrochlorothiazide (valsartan HCTZ) produced or distributed by Major Pharmaceuticals, Solco Healthcare, and Teva Pharmaceuticals Industries. Details about the products affected by the valsartan recall products are available through the FDA. ⚠️ USA RECALL ⚠️ The FDA has recalled Valsartan since it may be tainted by a substance that causes cancer and liver injuries. Valsartan, a drug manufactured in China treats high blood pressure and heart conditions.

Contact UsEditor’s note on the Valsartan Recall: This piece is written about the recent Valsartan Recall.

10 May 2019 More than a year before the FDA recalled tainted blood pressure drugs, an The valsartan recall came as little surprise to Massoud Motamed, 

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The valsartan recall came as little surprise to Massoud Motamed, a former inspector with the U.S. Food and Drug Administration (FDA). More than a year before the notices went out, Motamed had tried to sound the alarm on what he flagged as potential systemic problems at two facilities in China and India that produce the active ingredients in generic valsartan and other blood pressure medications.

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Valsartan recall

The federal agency stated that the medication to treat heart failure and high blood pressure contained a toxic chemical. Valsartan Recall Lawsuit The manufacturers of Valsartan are facing lawsuits after the drug was recalled for causing injury in some patients.
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Valsartan recall

Contact Us Editor’s note on the Valsartan Recall: This piece is written about the recent Valsartan Recall.

If you believe that what was alleged leading to the Valsartan Recall has affected you, please don’t hesitate to reach out to us. 41 rows 2019-3-13 · Since last summer, the FDA has issued a number of recalls of certain generic valsartan medications, which is used to treat high blood pressure and … A recall is underway across Europe following recent and emerging information that an impurity has been identified as part of the manufacturing process in a valsartan active substance manufactured 2018-9-24 · FDA has updated the list of valsartan products under recall and the list of valsartan products not under recall to incorporate additional repackagers of Camber’s valsartan products and Torrent’s recall. NDMA is a known environmental contaminant. For context, it is found in water and foods including meats, dairy products and vegetables.
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30 Oct 2019 The FDA had earlier recalled several types of blood pressure medications— losartan, valsartan, and irbesartan—because of contamination with 

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The voluntary valsartan recall specifically applies to certain valsartan and valsartan hydrochlorothiazide (valsartan HCTZ) produced or distributed by Major Pharmaceuticals, Solco Healthcare, and Teva Pharmaceuticals Industries. Details about the products affected by the valsartan recall products are available through the FDA.

2018-8-9 · The worldwide recall of drugs with the active ingredient valsartan continues to grow, with new companies being added to the list of participants. The U.S. Food and Drug Administration announced the initial U.S. recall in July 2018 involving three different companies that used Chinese manufacturer Zhejiang Huahai Pharmaceuticals. 2018-8-27 · FDA Issues a Recall Warning over Concerns That Some Valsartan is Contaminated With Carcinogens In July 2018, the FDA (Food and Drug Administration) began recalling drugs containing valsartan. The federal agency stated that the … A valsartan recall has been issued in 2018 due to the fact that the popular blood pressure and heart failure medication may have traces of a carcinogen. The U.S. Food and Drug Administration 2020-11-24 · The massive recall has also led to shortages of the important blood pressure drug and substantial price increases of non-recalled valsartan.

In a matter of mere months, the previously little-known pharmaceutical ingredient valsartan has gone from relative obscurity to being at the center of multiple drug recalls and at least one potential class-action lawsuit. Valsartan Lawsuit, Amlodipine Recall | Class Action?