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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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
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.
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.
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.
House Republicans Seek To Cut E-Cigarette Regulatory Funding For FDA June 23, 2015 Martha Garcia Add Your CommentsA controversial new bill approved by a U.S. House of Representatives subcommittee proposes to reduce the ability of the government to regulate e-cigarettes.ย House republicans are pushing to prevent FDA oversight on companies that sell e-cigs and other new tobacco products. However, many Democrats say this could allow products to remain on the market that could pose a risk of serious harm for children and other consumers.If passed, the proposed legislation would prevent the FDA from requiring pre-market approval for e-cigarette products that are already on the market. Effectively, it would allow all e-cigarettes a pass on FDA safety review.LEARN MORE ABOUTVAPE PEN AND E-CIG LAWSUITSSerious lung injuries, respiratory illnesses, and nicotine addiction have been linked to a wide range of vaping products, including e-cigarettes and THC vape pens. Lawsuits are being pursued against manufacturers for failing to warn users about these risks.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutVAPE PEN AND E-CIG LAWSUITSSerious lung injuries, respiratory illnesses, and nicotine addiction have been linked to a wide range of vaping products, including e-cigarettes and THC vape pens. Lawsuits are being pursued against manufacturers for failing to warn users about these risks.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONThe House subcommittee approved the measuresย Thursday, as part of a spending bill, and are sending it on for further approval by the full committee, the House, Senate and then the President.Under a rule currently proposed by the FDA, electronic cigarettes marketed before February 2007 would have to undergo retroactive pre-market approval, in addition to pre-market approval requirements for all new e-cigarettes and vaping devices. If this is the case, companies would have to submit applications within two years of the rule being finalized.The FDA would then review products to determine if they put the public at risk. If they do not meet that bar, they would be removed from the market.Republicans argue that a pre-market review would be a lengthy, expensive process that could drive many companies out of business.Alabama Representative Robert Aderholt, the bill’s sponsor, said the bill only seeks to have electronic cigarettes regulated in the same manner as tobacco. He also said it does not affect the FDAโs proposal to ban the sales of the products to minors and would still allow for other product standards.Many groups, including six U.S. Senators, have called on the FDA to place stricter regulations on e-cigarettes. The American Heart Association also called for more stringent guidelines for the industry, since the devices are appealing to adults and children alike.Eased Regulations, More Safety ConcernsThe new legislation would apply to other unregulated tobacco products, including cigars, hookahs, nicotine gels, water pipes tobacco, and dissolvable tobacco products. The FDA currently regulates cigarettes, smokeless tobacco and roll-your-own tobacco products.Public health safety groups say the bill would disrupt the FDAโs ability to prevent tobacco companies from marketing new products to children.Democrats say the bill would reduce regulation on the industry at a precarious time when many adults use e-cigarettes as a way to quit smoking tobacco cigarettes. Recently the use of e-cigarettes has increased rapidly as a result.Democrats also say the language of the House bill could keep products on the market that are targeted specifically toward teens, including cigars and e-cigarettes in candy-like fruit flavors, which new research has shown may cause respiratory health risks.New research indicates e-cigarette use by teens increased threefold in 2014. The U.S. Centers for Disease Control and Prevention warns that teens are increasingly vaping and millions of high school and middle school students are using the potentially dangerous devices.Nita Lowey, New York Democratic representative and top Democrat of the Appropriations Committee, called the bill a giveaway to the tobacco industry.The FDA’s proposed rules, which are expected to be finalized in a few months, are aimed at finally regulating the quickly growing e-cigarette industry. The tobacco companies downplay the effect the bill would have on the FDAโs regulatory authority. Yet, the FDA said the rules are important consumer protections. Written by: Martha GarciaHealth & Medical Research WriterMartha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: Congress, Electronic Cigarettes, Smokers, TobaccoMore JUUL E-Cigarette Vape Lawsuit Stories More Than Half of U.S. Teens Who Vape Do So To Deal With Stress, Anxiety: Study November 18, 2024 On-Line Retailers Receive FDA Warning Letter Over Illegal Sale of Disposable E-Cigarettes May 7, 2024 Vaping Causes Same DNA Damage as Smoking, Study Finds April 12, 2024 0 Comments NameThis 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 Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (Posted: today)The JPML has been asked to reject a petition by plaintiffs seeking to consolidate all federal Nevro spinal cord stimulator lawsuits before one federal judge, claiming the injuries and claims are too different from plaintiff to plaintiff.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026) Gulf War Veteran Parkinsonโs Disease Lawsuits Investigated Over Pesticide Use During Operations Desert Shield and Desert Storm (Posted: yesterday)Lawyers are investigating Parkinsonโs disease lawsuits for Gulf War veterans potentially exposed to the pesticide chlorpyrifos during Operations Desert Shield and Desert Storm.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITAgricultural Workers Face Higher Risk of ALS Due to Pesticide Exposure: Study (08/10/2026)Paraquat Exposure Lawsuit Claims Farm Herbicide Caused Parkinsonโs Disease (08/06/2026)Chlorpyrifos Pesticide Side Effects Research Highlights Decades of Parkinsonโs Disease Risks (08/04/2026) Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: 2 days ago)C.R. Bard and its Becton Dickinson parent company face more than 3,700 Bard PowerPort lawsuits that claim the port catheters are defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)
On-Line Retailers Receive FDA Warning Letter Over Illegal Sale of Disposable E-Cigarettes May 7, 2024
Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (Posted: today)The JPML has been asked to reject a petition by plaintiffs seeking to consolidate all federal Nevro spinal cord stimulator lawsuits before one federal judge, claiming the injuries and claims are too different from plaintiff to plaintiff.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)
Gulf War Veteran Parkinsonโs Disease Lawsuits Investigated Over Pesticide Use During Operations Desert Shield and Desert Storm (Posted: yesterday)Lawyers are investigating Parkinsonโs disease lawsuits for Gulf War veterans potentially exposed to the pesticide chlorpyrifos during Operations Desert Shield and Desert Storm.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITAgricultural Workers Face Higher Risk of ALS Due to Pesticide Exposure: Study (08/10/2026)Paraquat Exposure Lawsuit Claims Farm Herbicide Caused Parkinsonโs Disease (08/06/2026)Chlorpyrifos Pesticide Side Effects Research Highlights Decades of Parkinsonโs Disease Risks (08/04/2026)
Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: 2 days ago)C.R. Bard and its Becton Dickinson parent company face more than 3,700 Bard PowerPort lawsuits that claim the port catheters are defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)