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
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.
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.
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
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.
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.
AFFF Lawsuit Exposure to firefighting foam chemicals may result in an increased risk of cancer for firefighters, military and airport personnel.
Paraquat Parkinson’s Disease Lawsuits Exposure to the toxic herbicide Paraquat has been linked to a risk of Parkinson's disease.
Gardasil HPV Vaccine Lawsuit Side effects of the Gardasil HPV vaccine have been linked to reports of serious and debilitating autoimmune injuries. Lawyers review cases nationwide.
Monster Energy Drinks Will No Longer Be Labeled as Dietary Supplement February 14, 2013 Irvin Jackson Add Your Comments Monster energy drinks will soon be classified as a beverage, dropping the dietary supplement label, which has allowed the manufacturer to sell the drink without disclosing the amounts of caffeine and other stimulants it contains. The move comes after the manufacturer has faced sharp criticism amid mounting concerns about the risk of sever and potentially life-threatening health problems from Monster energy drinks. The labeling change was disclosed this week in Beverage Digest, an industry trade publication, after an interview with Monster Chief Executive Officer (CEO) Rodney Sacks. The change comes as the drink maker faces a number of lawsuits over Monster Energy, which allege that the beverage poses potential risks that are not adequately disclosed. The designation change means that Monster energy drinks will be qualified as a food item by the FDA, and will list “Nutritional Facts” instead of the current “Supplemental Facts.” The company will also reveal the caffeine content and will be restricted to ingredients that the FDA considers “generally recognized as safe.” Dietary Supplement Label Gives Manufacturers Wide Regulatory Leeway To date, Monster energy drinks have been classified as a dietary supplement, which allows the manufacturer to avoid FDA regulation. The designation also allows the manufacturer to sell the energy drink without listing the ingredients or conforming to other food safety regulations. Critics have indicated that Monster energy drinks are promoted as though they are a standard soft-drink or beverage, which leads to the assumption by consumers that there is federal oversight into the manufacture and composition. Because of the dietary supplement designation, the FDA has not required testing for the highly caffeinated energy drink to establish that it is safe for consumers. Many other energy drinks also use dietary supplement designations to avoid federal oversight. However, Red Bull, the second leading energy drink by volume after Monster, is already treated as a beverage. Concerns Raised Over Caffeine Side Effects Monster Energy and other competing products, such as Red Bull, Rockstar and 5 Hour Energy, combine high amounts of caffeine with other stimulants, such as guarana and taurine, to increase energy and stamina. However, concerns have emerged in recent years about the potential side effects of energy drinks may pose, especially among children and young adults who are typically encouraged to consume large amounts of the beverage. Research has found that caffeine overdose can result in heart attacks, cardiac arrhythmias and death after doses ranging from 200 to 400 milligrams, and Monster Energy drinks are aggressively promoted to teens and young adults, who often consume multiple cans in short periods of time to provide a “caffeine buzz” or induced burst of energy. The FDA has received at least 37 adverse event reports involving Monster drinks since 2004, including at least five deaths reported over the past year and a sixth reported in 2009. In October, a Monster Energy wrongful death lawsuit was filed by the family of a 14 year old girl who died from a cardiac arrest that was allegedly caused by a caffeine overdose after consuming two 24 ounce cans within a 24 hour period. Tags: Caffeine Overdose, Energy Drinks, Monster, Monster Energy, Red Bull, Rockstar Image Credit: | More Energy Drinks Lawsuit Stories 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 Case Report Links Kidney and Heart Failure To Energy Drink Consumption April 21, 2021 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 TermCommentsThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Hair Relaxer Wrongful Death Lawsuit Links Fatal Endometrial Cancer to Chemical Straightener Use (Posted: yesterday) A hair relaxer wrongful death lawsuit blames 16 years of using popular hair relaxer products like Just for Me and Dark & Lovely for the development of a fatal case of endometrial cancer. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Lawsuit Settlement Talks Begin With Focus on Finding Mediator, Parties Report (02/11/2025)Judge Indicates 40 Hair Relaxer Lawsuits Over Uterine Cancer, Endometrial Cancer and Ovarian Cancer Will Be Selected for Early Trial Program (02/03/2025)FDA Hair Relaxer Formaldehyde Ban Uncertain After All Pending Regulations Frozen: NBC Reports (01/24/2025) Depo-Provera Injury Lawyers To Apply for Leadership Positions in MDL (Posted: 2 days ago) Judge is calling for Depo-Provera lawyers to submit applications for MDL leadership by the end of the week, indicating that female attorneys should be adequately represented. MORE ABOUT: DEPO-PROVERA LAWSUITJudge Selects Five Depo-Provera Brain Tumor Lawsuits for “Pilot” Trials Weeks After MDL Established (02/25/2025)Depo-Provera Lawyers Will Meet With MDL Judge For Initial Case Management Conference on Friday (02/18/2025)Side Effects of Combined Hormonal Contraceptives Carry Higher Blood Clot Risks Than Others: Study (02/18/2025) Oxbryta Injury Lawsuit Over Discontinued Sickle Cell Disease Drug Set for Trial in June 2027 (Posted: 5 days ago) A federal judge has scheduled an Oxbryta lawsuit to go before a jury on June 7, 2027, which may be the first trial over side effects of the discontinued sickle cell disease drug. MORE ABOUT: OXBRYTA LAWSUITOxbryta Class Action Lawsuit Filed by Former Users of Sickle Cell Disease Drug Recalled in 2024 (12/30/2024)Lawsuit Alleges Oxbryta Side Effects Resulted in Higher Rate of Vaso-Occlusive Crisis, Other Debilitating Symptoms (11/19/2024)Oxbryta Recall Lawsuits Claim Drug Manufacturer Knew About Fatality Risks for Years (11/08/2024)
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
Hair Relaxer Wrongful Death Lawsuit Links Fatal Endometrial Cancer to Chemical Straightener Use (Posted: yesterday) A hair relaxer wrongful death lawsuit blames 16 years of using popular hair relaxer products like Just for Me and Dark & Lovely for the development of a fatal case of endometrial cancer. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Lawsuit Settlement Talks Begin With Focus on Finding Mediator, Parties Report (02/11/2025)Judge Indicates 40 Hair Relaxer Lawsuits Over Uterine Cancer, Endometrial Cancer and Ovarian Cancer Will Be Selected for Early Trial Program (02/03/2025)FDA Hair Relaxer Formaldehyde Ban Uncertain After All Pending Regulations Frozen: NBC Reports (01/24/2025)
Depo-Provera Injury Lawyers To Apply for Leadership Positions in MDL (Posted: 2 days ago) Judge is calling for Depo-Provera lawyers to submit applications for MDL leadership by the end of the week, indicating that female attorneys should be adequately represented. MORE ABOUT: DEPO-PROVERA LAWSUITJudge Selects Five Depo-Provera Brain Tumor Lawsuits for “Pilot” Trials Weeks After MDL Established (02/25/2025)Depo-Provera Lawyers Will Meet With MDL Judge For Initial Case Management Conference on Friday (02/18/2025)Side Effects of Combined Hormonal Contraceptives Carry Higher Blood Clot Risks Than Others: Study (02/18/2025)
Oxbryta Injury Lawsuit Over Discontinued Sickle Cell Disease Drug Set for Trial in June 2027 (Posted: 5 days ago) A federal judge has scheduled an Oxbryta lawsuit to go before a jury on June 7, 2027, which may be the first trial over side effects of the discontinued sickle cell disease drug. MORE ABOUT: OXBRYTA LAWSUITOxbryta Class Action Lawsuit Filed by Former Users of Sickle Cell Disease Drug Recalled in 2024 (12/30/2024)Lawsuit Alleges Oxbryta Side Effects Resulted in Higher Rate of Vaso-Occlusive Crisis, Other Debilitating Symptoms (11/19/2024)Oxbryta Recall Lawsuits Claim Drug Manufacturer Knew About Fatality Risks for Years (11/08/2024)