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
Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
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
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.
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.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
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.
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.
Energy Drink Marketing Should Be Examined by FTC: Congressman December 13, 2012 Irvin Jackson Add Your CommentsA U.S. lawmaker is calling on federal trade regulators to investigate the marketing practices involving popular energy drinks like Monster, Red Bull, Rockstar and 5 Hour Energy, claiming that the manufacturers appear to be heavily promoting the highly caffeinated beverages specifically to children, despite potential health risks of energy drinks.Late last month, Congressman Edward J. Markey, from Massachusetts, called on the Federal Trade Commission (FTC) to investigate energy drink manufacturers in a letter (PDF) sent to FTC Chairman Jon Leibowitz.The letter comes following recent FDA reports that linked dozen of deaths and other injuries to energy drinks.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATION“The advertising claims made by energy drink manufacturers are particularly alarming in light of the increase in advertisements targeted primarily to children and teenagers,” Markey wrote. “Accordingly, I believe an investigation of the claims made by these companies would fall within the [FTC’s] mandate…”Dietary Supplement Label Prevents FDA ReviewsMarkey notes that because the energy drinks are sold as dietary supplements, they do not fall under the FDA’s caffeine limitations for soft drinks, which restrict soda to 71 milligrams of caffeine per 12-ounce can. Some energy drinks can contain up to 500 milligrams of caffeine per serving.The dietary supplement label also prevents the FDA from reviewing whether the drinks are safe before they are placed on the market and sold to consumers, the letter points out.Some of the advertisements for energy drinks claim they prevent users from feeling tired, allow them to do more and make them more alert for hours; all claims which have never been substantiated by the FDA, Markey wrote.Last month, the City of San Francisco asked for documentation to support marketing claims regarding the safety of Monster Energy, after the manufacturer promoted the drinks to young adults with claims that users โcan never get too much of a good thing!โResearch has suggested that children and teens face a particularly high risk of experiencing energy drink side effects, as they commonly drink multiple beverages in a short period of time.In a 2011 study published in the medical journal Pediatrics (PDF), researchers estimated that 30% to 50% of adolescents and young adults consumer energy drinks and found that of the 5,448 caffeine overdoses reported in 2007, 46% of them involved youths under the age of 19.FTC Actions Led to Shut Down of Alcoholic Energy Drink IndustryThe FTC was the first agency to take action against the manufacturers of alcoholic energy drink, such as Four Loco and Joose, issuing a series of warning letters that ultimately led to the withdraw of drinks that combined high levels of caffeine with alcohol.The combination of alcohol and energy drinks was linked to a number of health risks, especially among underage drinkers and college students, often involving binge drinking and other reckless behavior. A 2007 study by researchers from Wake Forest University found that mixing alcohol, a depressant, and caffeine, a stimulant, can cause the drinker to be unaware of how intoxicated they actually are. The study found that college students who mixed caffeine and alcohol were more likely to be hurt, injured, ride with an intoxicated driver, or take advantage of someone else sexually.In late 2009, the FDA issued a letter to the manufacturers of alcoholic energy drinks, indicating that the practice of adding caffeine to alcoholic beverages fell under the control of the Federal Food, Drug and Cosmetic Act, and asked the manufacturers to provide evidence establishing that it is safe and legal. The move essentially resulted in the shut down of the alcoholic energy drink market.Reports of Deaths Lead to New Energy Drink InvestigationsThe recent focus on the health risks with non-alcoholic energy drinks has sharpened following the death of a 14-year-old girl who died after drinking two cans of Monster in 24 hours. Her family has since filed a wrongful death lawsuit against the makers of Monster in October 2012.According to the information released in recent weeks by the FDA, there have been at least four deaths linked to Monster Energy Drinks and 13 deaths linked to 5 Hour Energy Shots.ย In addition, side effects of Rockstar Energy Drinks have been cited in at least 13 non-fatal adverse event reports submitted to the FDA in recent years. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin 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. Tags: 5-Hour Energy, Caffeine Overdose, Energy Drinks, Four Loko, Monster, Rockstar 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 CommentsThis field is for validation purposes and should be left unchanged.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 NoPost Comment I authorize the above comments be posted on this pageWeekly 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 TermΔ MORE TOP STORIES Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (Posted: today)The second Bard PowerPort bellwether trial is now scheduled to begin in August after the plaintiff in a claim originally planned for trial next month died, and her family stopped pursuing litigation.MORE ABOUT: BARD POWERPORT LAWSUITJury Returns Defense Verdict in First Bard PowerPort Injury Lawsuit (05/11/2026)Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (04/16/2026)Judge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026) Dupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (Posted: yesterday)A Delaware woman has filed a Dupixent lawsuit, claiming manufacturers promoted the eczema drug as a breakthrough treatment while failing to warn that it may trigger or worsen CTCL, a rare form of non-Hodgkinโs lymphoma.MORE ABOUT: DUPIXENT LAWSUITLink Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026) Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: 2 days ago)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
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