logo
Girl Scouts of America Is Facing a Class Action Lawsuit That Threatens to Disrupt Beloved Cookie Season

Girl Scouts of America Is Facing a Class Action Lawsuit That Threatens to Disrupt Beloved Cookie Season

Yahoo12-03-2025
If you weren't aware of it already, it's officially Girl Scout cookie season. The nationally recognized (and quite frankly, obsessive) cookie season falls between January and April of each year, bringing with it loads of fan-favorite flavors for all to enjoy. Between Thin Mints, Samoas, Tagalongs, Trefoils, Do-si-dos, S'mores and Lemon-Ups, there's plenty of flavors to go around once the season begins.
Before we go too far down the favorite-flavor rabbit hole, there is one unfortunate bit of information that can potentially spoil this season's Girl Scout cookie madness: a class action lawsuit. That's right, our beloved Girl Scout cookies were just slapped with a federal lawsuit claiming that some cookies contain heavy metals, pesticides and other toxins.
The lawsuit, which was filed by a New York woman on Monday, certainly comes as bad timing for many, as it cites a study by 'Mom's Across America' and 'GMO Science,' claiming that 100-percent of cookies tested in the study contained toxins. It is important to note, however, that the study's claims are solely based on a small sample size of only 25 cookies across three states. So do with that information what you will.
Related:
In the meantime, there are some other factors that have been made clear in light of the lawsuit. For one, the study results were not peer-reviewed or published in a scientific journal. Additionally, the lawsuit seeks $5 million dollars in damages for people who brought the cookies across the United States. The lawsuit also calls for the cookie sellers to disclose the substances on packaging moving forward.
In response to the allegations made via the lawsuit, The Girl Scouts of America shared a blog post last month that the cookies are, in fact, 'safe to eat' and 'manufactured in line with all food safety regulations.' The company also added that heavy metals happen to occur naturally in soil where trace amounts are not a safety issue.
Related:
'Girl Scout Cookies are made with ingredients that adhere to food safety standards set by the FDA and other relevant authorities,' the blog post read. 'Our trusted bakers remain committed to compliance with all food safety standards and regulations set forth by the U.S. Food and Drug Administration (FDA), the Environmental Protection Agency (EPA), and other relevant health authorities.'
Until an official recall is on the books, we'll have to keep an eye on the situation as it develops. In our opinion, a study of more than just 25 cookies should be conducted, however it is pretty worrisome to learn that all 25 cookies tested positive for heavy metals and other toxins. There's definitely more to learn as the investigation progresses.
Up Next:
Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Novo Nordisk's Weight-Loss Drug Wegovy Approved to Treat Liver Disease
Novo Nordisk's Weight-Loss Drug Wegovy Approved to Treat Liver Disease

Yahoo

timean hour ago

  • Yahoo

Novo Nordisk's Weight-Loss Drug Wegovy Approved to Treat Liver Disease

Key Takeaways Novo Nordisk's blockbuster weight-loss drug, Wegovy, received Food and Drug Administration approval to treat a serious disease of the liver. Wegovy can be used for patients suffering from noncirrhotic metabolic dysfunction-associated steatohepatitis, or MASH. The company said MASH affects one in three overweight or obese people, including 22 million in the U.S. U.S.-listed shares of Novo Nordisk (NVO) gained 4% in premarket trading after the Food and Drug Administration (FDA) approved the pharmaceutical firm's popular weight-loss drug, Wegovy, to treat a serious liver disease. The Denmark-based firm reported the FDA said Wegovy could be used for adults suffering from noncirrhotic metabolic dysfunction-associated steatohepatitis, or MASH, who have moderate to advanced liver fibrosis, along with eating less and exercising more. Novo Nordisk Chief Scientific Officer Martin Holst Lange noted that the decision means Wegovy is the only GLP-1 obesity medicine that has received regulatory approval to treat MASH. He explained that one in three overweight or obese people suffer from it, with some 22 million Americans among them. He added that Wegovy not only stopped the disease activity, it also reversed liver damage. The company announced that Wegovy would be available immediately in the U.S. for the treatment of MASH. The approval is welcome news to Novo Nordisk investors, who have seen the U.S.-listed shares slump as competition from others in the weight-loss category has siphoned away sales of Wegovy. At the close of trading Friday, the shares were down nearly 40% year-to-date. Read the original article on Investopedia

HHS embraces AI
HHS embraces AI

Politico

timean hour ago

  • Politico

HHS embraces AI

EXAM ROOM The Department of Health and Human Services has emerged as the leader in artificial intelligence use among all federal agencies. In 2024, HHS reported 116 different ways to use AI for generating content and responses — up from just seven the year before, according to a report from the Government Accountability Office, which monitors agencies for Congress. The GAO reported 271 different AI tools in use last year. A recent analysis by the Bipartisan Policy Center, a think tank in Washington, reveals how three HHS agencies have implemented AI. Notably, they're largely using chatbots to help them work more efficiently. The Centers for Disease Control and Prevention: In 2023, the CDC launched ChatCDC, a bot built on OpenAI's large language models that can summarize meeting minutes, internal documents and studies. It also uses the bot to write code for data analysis. The CDC is experimenting with an updated version that uses more internal documents, but as of January, it hadn't yet been released. The Food and Drug Administration: The FDA has launched a chatbot to help staff respond to emails, summarize meeting minutes and perform a wide variety of basic tasks. While FDA Commissioner Marty Makary has promised faster regulatory review turnaround, staff have argued that the tool is prone to mistakes and incapable of assisting with the review process. The FDA has also experimented with using AI for an array of tasks, including labeling drugs and looking for data patterns and anomalies. The Centers for Medicare and Medicaid Services: CMS uses AI to prevent and detect fraud, waste and abuse and analyze prescription drug costs. The takeaway: HHS continues to lead the way for AI use. Health Secretary Robert F. Kennedy Jr. has said he sees digital technology and AI as key tools for improving health care outcomes and reducing costs. WELCOME TO FUTURE PULSE This is where we explore the ideas and innovators shaping health care. Sen. Marsha Blackburn (R-Tenn.) is calling for an investigation into Meta following reporting that the company allowed its chatbots to 'engage a child in conversations that are romantic or sensual.' Share any thoughts, news, tips and feedback with Carmen Paun at cpaun@ Ruth Reader at rreader@ or Erin Schumaker at eschumaker@ Want to share a tip securely? Message us on Signal: CarmenP.82, RuthReader.02 or ErinSchumaker.01. INFLUENCERS A newly launched psychedelic medicine foundation wants to become the 'American Cancer Society of ibogaine access.' Mission Within Foundation, which officially launched today, plans to use the $2 million in funding it has secured from private donors and foundations to promote the psychedelic drug ibogaine, derived from an African shrub, as a mental health treatment. The Drug Enforcement Administration classifies ibogaine as a Schedule I drug with no currently acceptable medical use and a high risk of abuse. It can pose heart risks and has been linked to about two dozen deaths in recent decades. The foundation plans to lobby for safe and legal access to ibogaine treatment in the U.S. and offer fully funded psychedelic therapy retreats to veterans and frontline workers with post-traumatic stress disorder, traumatic brain injuries, depression and addiction. It will also team up with the Dell Medical School at the University of Texas on three ibogaine research studies. Who's who: Dr. Martín Polanco, who runs The Mission Within, a psychedelic medicine clinic in Tijuana, Mexico, is one of the foundation's founders. He's treated more than 5,000 people with traumatic brain injuries and mental health conditions like PTSD, including many veterans, using ibogaine and the psychedelic drug 5-MeO-DMT, a desert toad secretion. Polanco has the ear of Reps. Jack Bergman (R-Mich.) and Lou Correa (D-Calif.), co-founders of the Congressional Psychedelics Advancing Therapies Caucus, who've been working in Washington to advance psychedelic medicine. Correa traveled to Polanco's clinic in Tijuana last year to talk with him in person and see whether his work justified further research on the drugs in the U.S. The foundation, which is also advocating for psychedelic medicine more broadly, is supporting Correa and Bergman's Innovative Therapies Centers of Excellence Act, which the pair introduced in April. The bill seeks $30 million for Veterans Affairs Department research on psychedelic therapies and would create five centers of excellence to research alternative treatments for veterans. What's next: Texas Gov. Greg Abbott, a Republican, signed a law in June putting $50 million in state funding toward clinical trials of ibogaine as a mental health treatment. And the state budget Arizona's Democratic governor, Katie Hobbs, signed into law the same month included a commitment of $5 million for studying ibogaine. Mississippi plans to hold a joint hearing of the House and Senate Public Health and Human Services committees on ibogaine on August 28.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store