RoundUp Lawsuit

As Monsanto’s flagship product, the weed killer Roundup generates approximately $5 billion in annual sales for the company. In March of 2015, the International Agency for Research on Cancer (IARC), part of the highly respected World Health Organization, reported that Roundup contains a probable cancer causing chemical called glyphosate. Cases of persons suffering from the cancer known as non-Hodgkin lymphoma caused by exposure to Roundup have been filed and consolidated in a federal court Multi-District Litigation (MDL) in San Francisco. Documents produced in the MDL show that Monsanto desperately tried to hide information about the dangers of Roundup from the public in the form of falsified studies and protection from government agencies.

IARC’s report exposing Roundup’s glyphosate as a probable cause of cancer was supported by numerous scientific research studies. In particular, research studies, including one conducted as early as 2002, found an association between glyphosate and the cancer known as non-Hodgkin lymphoma. Faced with the damning evidence published by IARC, Monsanto struck back with a vengeance. Monsanto approached various regulatory departments of United States governmental agencies for the purpose of keeping information about its cancer causing Roundup a secret. Documents produced in the federal court MDL show that the Environmental Protection Agency (EPA) and the Department Health and Human Services conspired with Monsanto to hide Roundup’s glyphosate connection with causing cancer. Additionally, Monsanto conducted fraudulent studies designed to deceive governmental agencies and the public into concluding that Roundup’s glyphosate is safe and does not cause cancer. Monsanto submitted its phony studies to the EPA. Based on these studies, the EPA initially reported that Roundup’s glyphosate was “not likely to be carcinogenic,” but were later forced to remove this unsupported statement from the EPA website.

Monsanto’s dishonest effort to keep their carcinogenic product Roundup on the market displays a clear disregard for human life. Roundup constitutes one third of Monsanto’s sales revenues, leaving little doubt as to the motive for their shameful behavior. However, despite its power as a big corporation, Monsanto’s day of reckoning may not be far off. To date, more than 50 cases have been filed against Monsanto for cancer caused by Roundup in state and federal courts. The federal cases have all been consolidated into one Multi-district Litigation in San Francisco. The Monsanto Roundup litigation continues to grow, as lawsuit filings are increasing. It is anticipated that this litigation will ultimately grow to include thousands of cases and they will collectively hold Monsanto responsible for destroying countless lives for the sake of profit.

Roundup remains on the market as a product commonly used by many Americans, including farmers, landscapers, and gardeners. While the use of this toxic herbicide product remains common, its lesser known cancer causing risks are quickly coming to light.

If you or a loved one has non-Hodgins lymphoma cancer that may have been caused by exposure to Roundup, the experienced Mass Tort lawyers at The Yost Legal Group are here to help. Call The Yost Legal Group today at 1-800-YOST-LAW (967-8529) for a FREE, confidential, no-obligation consultation. At The Yost Legal Group, there is no fee or expense unless you recover.

FDA’s Black Box Warning Labels Essure as Dangerous Device

The FDA announced on Monday, 2/29 that it will recommend a “black box warning” label for the Essure permanent birth control device. According to the FDA website, a black box warning label is “designed to call attention to serious or life-threatening risks” associated with a prescription drug or medical device. The FDA also instructed Essure manufacturer Bayer Pharmaceuticals to conduct additional studies in order to better understand the risks of prescribing this permanent contraception device to women.

The Essure permanent contraception device was approved by the FDA in 2002 and marketed as a non-surgical, permanent birth control solution for women. Bayer Pharmaceuticals, the manufacturers of the Essure implant, told women that this device would be a safe and effective alternative to laparoscopic sterilization.

According to Reuters, there are more than 500,000 women in the United States that are using the Essure device. Since 2002, the FDA has received more than 5,000 serious injury complaints from women using this device. These women have reported device failures, such as fracturing or migration inside the body, as well as autoimmune responses, such as unexplained but significant weight gain, skin conditions, hair loss and abnormally heavy menstrual cycles.

If you suffered injuries after receiving an Essure implantable sterilization device and want to learn more about your legal options, call The Yost Legal Group at 1-800-YOST-LAW (967-8529). When you call, you will speak with one of our experienced Defective Medical Device attorney absolutely FREE.

The attorneys at The Yost Legal Group are experienced professionals ready to investigate your claim with compassion and determination. Call today for a free consultation.

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