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.
Wrigley Temporarily Recalls Alert Energy Gum Amid FDA Concerns May 9, 2013 Irvin Jackson Add Your CommentsJust days after introducing Alert Energy gum, Wrigley has halted production and sales for its caffeine gum, as federal health regulators are reviewing concerns about the safety of adding caffeine to gum and candy.On May 8, Wrigley announced that it was pausing production, sale and marketing of Alert Energy Caffeine Gum in response to discussions with the FDA, which had launched an investigation into the gum’s safety.The FDA has indicated that it is concerned over the rampant addition of caffeine to everything from waffles to jelly beans, many of which are likely to be used by children.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 COMPENSATIONWrigley, a subsidiary of Mars, launched Alert on April 29, sparking an immediate response from the FDA. The agency vowed to investigate the safety of caffeine in all food products, especially those targeting children. FDA officials said one pack of the gum was like carrying four cups of coffee in your pocket.Alert gum contains 40 mg of caffeine in each stick, which is the equivalent of about half a cup of coffee.“The FDA applauds Wrigley’s decision and its recognition that we need to improve understanding and, as needed, strengthen the regulatory framework governing the appropriate levels and uses of caffeine in foods and beverages,” said Michael R. Taylor, FDA Deputy Commissioner for Foods and Veterinary Medicine. “The company’s action demonstrates real leadership and commitment to the public health. We hope others in the food industry will exercise similar restraint.”The actions come amid ongoing concerns about the health risks of caffeinated energy drinks, which have been linked to a large number of adverse event reports submitted to the FDA involving heart problems and even deaths.A 14 year old California girl suffered cardiac arrest last year, allegedly caused by caffeine overdose after drinking two Monster Energy drinks over a 24 hour-period. Her parents are currently pursuing aย lawsuit against Monster Energy Corp.Many medical organizations warn that caffeine can have far reaching side effects for children, who cannot process caffeine as sufficiently as adults.ย Theย American Academy of Pediatricsย warns that caffeine may cause neurologic and cardiovascular problems in children. 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: Caffeine Overdose, Children, Energy Drinks, WrigleyMore 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 2 Comments Kathi March 6, 2020 I believe Alert caffeine gum is the best gum ever. I have my family, they come to visit 2 years of being able to play with 2 children, 5 grand children, and 6 great grand children. Alert gum has helped me to be caffeinated, and enjoy my life. I had surgery, gastric bypass, so I canโt drink coffee it causes terrible pain in my stomach, but Alert gum does not affect my sensitivity in any way. I chew both mint and fruit flavor. I canโt find it in the stores anymore idk why. I order it through the mail and the mint gum is becoming hard to find, but I find it. Also MEG sticks to my dentures, I stick with my Alert gum and feel good. 2 yrs of Alert gum still moving along. I have introduced Alert gum to family and friends from NJ all the way to Fla. Iโm gonna keep on going. jackie May 10, 2013 I purchased a pack of this Alert Gum on Thursday, May 2, 2013. I chewed a piece on Saturday, May 4, 2013. After an hour I was hallucinating and thought there was a bird flying around in my house. Scary stuff. 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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 Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: yesterday)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026) Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 2 days ago)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link 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) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 3 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)
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