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As Paraquat Parkinson’s Disease Cases Continue To Emerge, Syngenta Will Halt Herbicide’s Production

As Paraquat Parkinson's Disease Cases Continue To Emerge, Syngenta Will Halt Production

The agricultural technology company Syngenta announced last week that it is ending production of the controversial weed killer Paraquat in June 2026, after years of litigation against the company over the failure to adequately warn that users may be at risk of developing Parkinson’s disease, even when all of the recommended safety features are followed.

Paraquat was first approved for use in the United States in 1964, when it was sold under the brand name Gramoxone. Although it has been banned in more than 70 countries due to its extreme toxicity, it remains widely used in the U.S. to kill broadleaf weeds and grasses before crops are planted. It is also used after harvest to dry out certain crops.

The herbicide has long been associated with severe poisoning risks and, in recent years, researchers have also linked exposure to Parkinson’s disease. Studies indicate that farm workers, landscapers and others who regularly spray, mix or handle the herbicide may face a higher risk of developing chronic and progressive neurological damage.

As a result, manufacturers now face thousands of Paraquat lawsuits in federal court alleging that Syngenta failed to warn users that the herbicide may increase the risk of Parkinson’s disease.

Syngenta Ends Paraquat Production

On March 3, Syngenta issued a press release announcing that it was ending global production of Paraquat. The company currently plans to phase out production by June of this year and plans to retool the only Paraquat manufacturing plant in Huddersfield, UK.

While the company still maintains that Paraquat is safe and effective, and claims it has chosen to move on to new technologies, the announcement comes as lawmakers in several states call for the weed killer to be banned, including Pennsylvania, Illinois, Missouri, New Jersey, Vermont, Virginia, Washington, West Virginia and Utah.

“This decision is about focusing our resources where they deliver the greatest value for our business and our customers.”

– Mike Hollands, President of Syngenta UK, and head of global production and supply

The press release states that the company will work with customers to assist in transitioning away from Paraquat use.

Paraquat Parkinson’s Disease Lawsuits

The decision to end production also comes as plaintiffs and defendants in more than 6,000 Paraquat lawsuits continue to work to finalize terms of a global settlement agreement to compensate former users diagnosed with Parkinson’s disease.

Since June 2021, all federal Paraquat lawsuits have been consolidated as part of a multidistrict litigation (MDL) in the Southern District of Illinois, where U.S. District Judge Nancy Rosenstengal has been working with the parties to prepare for a series of early “bellwether” trials, which are designed to gauge how juries may respond to evidence and testimony likely to be repeated throughout the litigation.

The first trial was expected to begin in January 2026. However, Syngenta reached a settlement agreement with the plaintiff, avoiding the trial at the last minute. The settlement came after attorneys announced in April 2025 that they were nearing a Paraquat Parkinson’s disease lawsuit settlement agreement to resolve all claims pending in the federal MDL. Judge Rosenstengal subsequently put a stay in place on all pretrial proceedings at the federal level. In December, she extended the Paraquat lawsuit stay until March 6, 2026.

To stay up to date on this litigation, sign up to receive Paraquat lawsuit updates sent directly to your inbox.

Image Credit: Shutterstock.com / Taljat David
Written By: Irvin Jackson

Senior Legal Journalist & Contributing Editor

Irvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends.



1 Comments


Jamie
My wife was diagnosed with Parkinson’s Disease at age 62. She had severe calf pain, muscle pain, tremors, slurred speech, frequent falls, loss of balance, and difficulty getting up from a sitting position. She was put on Sinemet for 6 months, and then Siferol was introduced and replaced the Sinemet. Neither standard treatment like B1 and high dose B12 did very little for her. We tried different supplements that didn’t work, so last August, our family doctor started her on the PD-5 protocol—the best decision ever! 2 months into treatment she improved dramatically. At the end of the full treatment course, the disease is totally under control. Cases of muscle weakness, constant twitches and tremors eased. My wife has resumed her daily activities. As I share this experience, she’s active again. I’m surprised a lot of PWPs haven’t heard of the PD-5 protocol. We got the protocol from ww w. Limitlessnaturalwellness .com

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