FDA Investigating Panera Bread “Charged Lemonade” After Wrongful Death Lawsuit Filed Over Fatal Cardiac Arrest
PRIME, 5-Hour Energy Drink Recall Issued In Canada, as U.S. Senator Calls for Investigation into Caffeine Levels
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
AngioDynamics Port Catheter Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
New Beverage Guidelines Say Some Supplement Additives Fall Under FDA January 15, 2014 Martha Garcia Add Your Comments The FDA issued long anticipated guidance this week for dietary supplements and beverages, including controversial energy drinks that have raised concerns about how the manufacturers of the highly caffeinated beverages have been able to largely avoid federal regulation by categorizing their products as supplements. The guidelines are aimed at clarifying the role of certain dietary supplements, which are substances added to foods and beverages, focusing on the of energy drinks. Manufacturers of energy drinks have been able to avoid disclose details about the contents and levels of caffeine contained in their products because they are usually classified as dietary supplements. However, the new guidance hopes to evaluate each liquid product on an individual basis before determining whether it falls under dietary supplement guidelines or should be categorized as a food product, which include a beverage subcategory. Learn More About Energy Drink Lawsuits Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Energy Drink Lawsuits Learn More SEE IF YOU QUALIFY FOR COMPENSATION The guidelines indicate the FDA will focus on how the product is marketed, including graphics on the product, product labels, websites and social media. This is meant to evaluate how the product is represented and how the product is intended to be used. Late last year, Monster Beverage Corp. proposed industry marketing guidelines to the American Beverage Association, but refused to release details of the plans to the public. The secret guidelines were drafted to address the concerns about the aggressive marketing of energy drinks that are often directed at children. However, the company indicated that it will only adopt the guidelines if all energy drink makers, including makers of Red Bull, Rock Star, 5-Hour Energy and others, agree to adopt the voluntary industry guidelines as well. Other factors that will also be considered in the new FDA guidance are whether the product claims to “refresh” or “hydrate” the consumer. The FDA indicates products that advertise such claims are being represented as a beverage, not a dietary supplement, as many energy drink makers claim. Monster announced in February 2013 that it would drop the dietary supplement facts panel and begin to classify their products as beverages, voluntarily placing them under FDA regulations. The move means Monster relinquishes its right not to withhold information about the amounts of caffeine and other stimulants in its products. However, the decision came only after the manufacturer faced strong criticism about their marketing and concerns about the potental risk of life-threatening health problems linked to Monster energy drinks. While the step was voluntary in the case of Monster, many other energy drinks might soon be required to follow suit under the new FDA guidelines. The FDA said it was up to manufacturers to make sure the substances added to foods and used in dietary supplements comply with the regulatory requirements set forth by the agency. The guidance also highlights if a product is not generally recognized as safe (GRAS) by food experts, showing scientific evidence of reasonable safety, it will be considered a food additive and will require premarket approval by the FDA. The FDA warns many substances which have not been previously used in conventional foods may be unapproved as food additives. Other substances have been present in the food supply, but are now being added to foods and beverages in amounts in excess of traditional use levels. In many instances, high levels of caffeine and other substances used in energy drinks. “This trend raises questions as to whether these higher levels and other new conditions of use are safe,” agency officials stated recently. Tags: Caffeine Overdose, Dietary Supplement, Energy Drinks, Monster Image Credit: | More Energy Drinks Lawsuit Stories Taurine Found in Energy Drinks May Increase Blood Cancer Risks: Study May 20, 2025 FDA Investigating Panera Bread “Charged Lemonade” After Wrongful Death Lawsuit Filed Over Fatal Cardiac Arrest October 26, 2023 PRIME, 5-Hour Energy Drink Recall Issued In Canada, as U.S. Senator Calls for Investigation into Caffeine Levels July 13, 2023 0 Comments Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes No Post Comment I authorize the above comments be posted on this page Weekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings. Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermPhoneThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Lawsuit Alleges Depo-Provera DMPA Injection Increases Brain Tumor Risks (Posted: yesterday) A Depo-Provera lawsuit blames the active ingredient, DMPA, for an increased risk of the development of brain tumors. 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FDA Investigating Panera Bread “Charged Lemonade” After Wrongful Death Lawsuit Filed Over Fatal Cardiac Arrest October 26, 2023
PRIME, 5-Hour Energy Drink Recall Issued In Canada, as U.S. Senator Calls for Investigation into Caffeine Levels July 13, 2023
Lawsuit Alleges Depo-Provera DMPA Injection Increases Brain Tumor Risks (Posted: yesterday) A Depo-Provera lawsuit blames the active ingredient, DMPA, for an increased risk of the development of brain tumors. MORE ABOUT: DEPO-PROVERA LAWSUITOrtho-Cept, Similar Birth Control Pills Linked to Intracranial Meningioma Risks, Study Warns (06/17/2025)Status of Depo-Provera Shot Lawsuits Outlined by MDL Judge (06/13/2025)Pfizer Requests Depo-Provera Lawsuit Coordination as Mass Tort in Pennsylvania State Court (06/10/2025)
Zantac Cancer Lawsuits Continue To Be Filed More Than 5 Years After Recall (Posted: 3 days ago) A man diagnosed with multiple forms of cancer has filed a Zantac lawsuit, blaming Boehringer Ingelheim for failing to adequately warn about the recalled heartburn drug’s health risks. MORE ABOUT: ZANTAC CANCER LAWSUITSJury Hears Zantac Cancer Evidence in Illinois Trial Against Boehringer Ingelheim (02/05/2025)Zantac Bladder Cancer Lawsuit Trial Ends With Hung Jury in California (11/22/2024)GSK To Pay $2.2 Billion To Settle Zantac Cancer Lawsuits Brought by 80,000 Consumers (10/10/2024)
Enfamil NEC Lawsuit Filed After Newborn Suffers ‘Nearly Total Bowel Necrosis’ (Posted: 4 days ago) Necrotizing enterocolitis caused by Enfamil resulted in a newborn suffering life-long bowel injuries, according to a lawsuit filed by his mother. MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITReckitt Benckiser Faces Class Action Lawsuit Over Enfamil NEC Risks (06/12/2025)NEC Infant Formula Lawyers To Meet With MDL Judge Following Dismissal of First Bellwether Trial (05/29/2025)FDA To Investigate Whether Infant Formula Products Provide Enough Nutrition (05/16/2025)