FDA Investigating Panera Bread “Charged Lemonade” After Wrongful Death Lawsuit Filed Over Fatal Cardiac Arrest
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.
PRIME, 5-Hour Energy Drink Recall Issued In Canada, as U.S. Senator Calls for Investigation into Caffeine LevelsPRIME, heavily marketed toward youth on social media, contains as much caffeine as six cans of normal Coca Cola, investigators found. July 13, 2023 Irvin Jackson Add Your CommentsCanadian health officials have issued a recall for several popular energy drink brands, including PRIME and 5-Hour Energy, as U.S. law makers are also raising concerns about the high levels of caffeine in certain products.The Canadian Food Inspection Agency (CFIA) announced the energy drink recall on July 12, impacting products sold under the brand names PRIME, 5-Hour Energy, 3D Alphaland, Celsius, GFuel and Sting, which the regulators indicate violate laws in Canada linked to caffeine content and how those cans should be labeled. The recalls appear to affect only those without labels in both English and French.The warning indicates the recalled energy drinks should not to be consumed, sold, served or distributed in Canada. A full list of the affected energy drinks is included in the recall notice, and were sold both nationally and online.The CFIA is recommending Canadian consumers check to see if they have the affected products, and not to consume them if they do. The agency also asks consumers who see the products being sold to report such incidents to the CFIA and to contact their healthcare provider if they consume one and begin to feel ill. The recall came after agency inspections, which are ongoing and may lead to additional recalls.Energy Drink Health ConcernsAlthough most consumers believe energy drinks to be safe due to information on the nutrition labels, the drinks are not regulated in the U.S. because they are considered dietary supplements. Many manufacturers do not even disclose the ingredients or levels of caffeine contained in each bottle.Amid aggressive marketing by the manufacturers, energy drink sales increased 240% between 2004 and 2009, and the number ofย caffeine overdose emergency room visitsย increased from 1,128 in 2005 to 16,055 in 2008. Approximately 56% of those visits involved individuals between the ages of 12 and 25 years.In March 2016, the American Heart Association indicated that theย overuse of energy drinks could cause increased heart problemsย including heart attacks, sudden cardiac arrest and other potentially life-threatening complications.A major concern regarding energy drinks involves the high levels of caffeine found in many brands. PRIME, for example, which had been distributed in Canada but not yet released for sale, contains about 200 milligrams of caffeine per can, which is about the same amount found in six cans of Coca Cola, which exceeds Canadaโs 180 mg limit on caffeine per serving.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 COMPENSATIONU.S. Senator Calls for PRIME Energy Drink InvestigationAs Canadian officials recalled PRIME energy drinks, U.S. law makers are calling for a similar investigation.On Sunday, U.S. Senate Majority Leader Chuck Schumer called for the U.S. Food and Drug Administration (FDA) to also launch an investigation into PRIME, which hit the market in the U.S. last year, due to the energy drinkโs high caffeine levels.Schumer called for the investigation at a press conference held on Sunday, warning that the drinkโs popularity on social media and with youth raise concerns about the health risks. The drinks are not recommended for children under 18 years old, but have been released in youth-friendly flavors and promoted by social media influencers like Logan Paul and KSI, which has helped make the drinks extremely popular and even hard to keep on store shelves in the U.S., U.K. and Australia.PRIME is now the official sports drink of several popular sports teams, like the Los Angeles Dodgers, increasing its visibility.High levels of caffeine have been linked to irregular heartbeats in some consumers, resulting in increased blood pressure, heart arrhythmias, fainting, seizures and sudden death, particularly in younger consumers.The FDA has yet to say if it will launch such an investigation. 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, Canada, Congress, Energy Drink Recall, Energy Drinks, PrimeMore 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 Case Report Links Kidney and Heart Failure To Energy Drink Consumption April 21, 2021 1 Comments Monty July 24, 2023 “…..the drinks are not regulated in the U.S. because they are considered dietary supplements.” Dietary supplements are regulated as found in the Code of Federal Reulations, Title 21 ,Chapter 1, Subchapter B, Part 111 PhoneThis 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 Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (Posted: yesterday)According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026) Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (Posted: 2 days ago)A Depo-Provera intracranial meningioma lawsuit claims Pfizer developed and sold a defective birth control injection that puts women at a five times increased risk of brain tumors.MORE ABOUT: DEPO-PROVERA LAWSUITLawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026) Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (Posted: 3 days ago)A lawsuit alleges an Illinois woman developed CTCL after using Dupixent, raising concerns the manufacturer may have withheld concerns that the drug could contribute to cancer.MORE ABOUT: DUPIXENT LAWSUITLawsuit 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)Dupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)
FDA Investigating Panera Bread “Charged Lemonade” After Wrongful Death Lawsuit Filed Over Fatal Cardiac Arrest October 26, 2023
Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (Posted: yesterday)According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)
Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (Posted: 2 days ago)A Depo-Provera intracranial meningioma lawsuit claims Pfizer developed and sold a defective birth control injection that puts women at a five times increased risk of brain tumors.MORE ABOUT: DEPO-PROVERA LAWSUITLawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)
Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (Posted: 3 days ago)A lawsuit alleges an Illinois woman developed CTCL after using Dupixent, raising concerns the manufacturer may have withheld concerns that the drug could contribute to cancer.MORE ABOUT: DUPIXENT LAWSUITLawsuit 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)Dupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)