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.
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.
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.
FDA Warns Caffeine Powder Distributors To Stop Selling Deadly Doses September 2, 2015 Irvin Jackson Add Your Comments Federal health regulators are warning distributors that they are selling deadly doses of powdered caffeine, which have resulted in a number of deaths and serious injuries. On August 27, the FDA issued five warning letters to distributors of caffeine powder, including PureBulk, of Roseburg, Oregon; Kreative Health Inc., doing business as Natural Food Supplements, of Conoga Park, California; Smartpowders, of Graham, North Carolina; Hard Eight Nutrition LLC, of Henderson, Nevada; and Bridge City LLC, of Portland, Oregon. According to the letters, the companies are sending out dietary supplements that present “a significant or unreasonable risk of illness or injury under the conditions of use recommended or suggested in the labeling.” Do You Know about… hair dye cancer lawsuits For Salon Professionals Hair dye lawsuits are being pursued for salon professionals who were routinely exposed to hair dye chemicals and diagnosed with bladder cancer or breast cancer. See if you qualify for a hair dye cancer lawsuit settlement. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know About… hair dye cancer lawsuits For Salon Professionals Hair dye lawsuits are being pursued for salon professionals who were routinely exposed to hair dye chemicals and diagnosed with bladder cancer or breast cancer. See if you qualify for a hair dye cancer lawsuit settlement. Learn More SEE IF YOU QUALIFY FOR COMPENSATION The FDA warns that the caffeine powder is so dangerous that consumers put their lives at risk if they deviate from the recommended dosages by the smallest amount, and warns that most consumers do not have a scale or measuring device significantly accurate to safely measure the proper dosage. The FDA notes that the safe amounts are, at their largest, 1/14th of a teaspoon. Many of the distributors are selling packages that hold 25 grams to 25 kilograms of caffeine powder. “Caffeine is a powerful stimulant. A single teaspoon of pure powdered caffeine is roughly equivalent to the amount of 28 cups of coffee,” the warning letters indicate. “Consuming as little as one teaspoon of caffeine has been associated with symptoms including nausea, vomiting, anxiety, and heart palpitations.” Consuming an entire tablespoon can lead to heart problems and death, the agency warns. The agency warned the companies to respond in 15 working days to correct the violations and explain how they will make their products safe for consumer use. Failure to do so could result in the seizure of their inventory or a court injunction. Caffeine Powder Concerns The warning letters came following the urging of U.S. Senator Sherrod Brown, a democrat from Ohio and a number of other senators. They have asked the agency to require better labeling and to ban the retail sale of caffeine powder altogether. Senator Brown issued a press release on September 1 after the FDA sent out the letters. “Even a small amount of powdered caffeine can injure and even kill those who accidently ingest too much. But too many who use it don’t know its risks,” Brown said in the press release. “Today’s action by the FDA will help protect consumers from this dangerous product. By requiring distributors of powdered caffeine to revise their labels and provide accurate and complete information to consumers, we can help save lives. While these warning letters are is a step in the right direction toward protecting consumers, I’ll continue my push to ban this product for retail sale.” In July 2014, the FDA issued a safety advisory about the potential health risks with powdered caffeine, warning consumers to avoid using the products after they were linked to reports of serious injury and death. A recent investigation by the FDA has also shown an increase in hospitalizations from caffeine toxicity reported across the country in recent years, stemming from the use of energy drinks, shots and other products containing high amounts of caffeine and other stimulants. With the popularity of pure powdered caffeine growing, the FDA has recorded an increased number of hospitalizations from toxic caffeine levels in younger generations across the country in recent years. Many of the cases are directly related to the use of energy drinks, energy shots, and other harmful caffeine stimulants labeled as “All Natural.” Symptoms of caffeine overdose can begin by feeling flushed which includes a rapid or dangerously erratic heartbeat, vomiting, diarrhea, disorientation, and at extremely dangerous levels may cause seizures leading to death. At least one caffeine powder wrongful death lawsuit has been filed against companies that have distributed the products, including Amazon.com. The complaint was filed by the family of Logan Stiner earlier this year, after Stiner died of a powdered caffeine overdose last year after using powder he ordered online. The FDA is asking that consumer stop using pure caffeine powder products immediately to avoid possible overdose and death. Consumers should warn their peers about the dangers of these products and report any adverse health consequences to the FDA at 240-402-2405 or by email at CAERS@cfsan.fda.gov. Tags: Caffeine Overdose, Caffeine Powder, Congress, Wrongful Death Lawsuit More Lawsuit Stories Court Urged To Reject Motion To Dismiss Lawsuits Over Ozempic, Mounjaro Gastrointestinal Risks March 21, 2025 McKesson Sterile Water Lawsuit Filed Against Amazon, Nurse Assist Over Bacterial Wound Infection March 21, 2025 Elevidys Side Effects Suspected in Liver Failure, Death of Duchenne Muscular Dystrophy Patient March 21, 2025 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 Court Urged To Reject Motion To Dismiss Lawsuits Over Ozempic, Mounjaro Gastrointestinal Risks (Posted: today) Pushing back against a motion to dismiss, plaintiffs involved in GLP-1 lawsuits say GLP-1 manufacturers intentionally misled the medical community and patients regarding the safety of the diabetes and weight loss drugs. 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Court Urged To Reject Motion To Dismiss Lawsuits Over Ozempic, Mounjaro Gastrointestinal Risks March 21, 2025
McKesson Sterile Water Lawsuit Filed Against Amazon, Nurse Assist Over Bacterial Wound Infection March 21, 2025
Elevidys Side Effects Suspected in Liver Failure, Death of Duchenne Muscular Dystrophy Patient March 21, 2025
Court Urged To Reject Motion To Dismiss Lawsuits Over Ozempic, Mounjaro Gastrointestinal Risks (Posted: today) Pushing back against a motion to dismiss, plaintiffs involved in GLP-1 lawsuits say GLP-1 manufacturers intentionally misled the medical community and patients regarding the safety of the diabetes and weight loss drugs. MORE ABOUT: OZEMPIC LAWSUITGLP-1 Manufacturers Argue Gastroparesis Lawsuits Should Require Contemporaneous Diagnostic Testing (03/17/2025)Study Suggests There May Not Be a Link Between Ozempic, Mounjaro and Post-Surgery Aspiration Pneumonia (03/12/2025)Ozempic Hair Loss Side Effects Doubled for Users, Study Finds (03/07/2025)
McKesson Sterile Water Lawsuit Filed Against Amazon, Nurse Assist Over Bacterial Wound Infection (Posted: today) An Arizona man contends that the manufacturers delayed issuing a recall of sterile water products sold on Amazon, resulting in a serious infection requiring multiple surgeries. MORE ABOUT: STERILE SALINE SOLUTION RECALL LAWSUITSteriCare Sodium Chloride Lawsuit Claims Recalled Saline Solution Caused Infection, Wrongful Death (11/12/2024)Nurse Assist Sterile Water and Saline Recalled Following FDA “Do Not Use” Warning (11/07/2023)
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