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.
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.
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.
Tabletop Fire Pit Lawsuit Individuals who suffered severe burns, or families who lost a loved one in a tabletop fire pit explosion, may be eligible for financial compensation through a fire pit injury lawsuit.
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.
Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
Ocaliva Lawsuit Ocaliva lawsuits are being investigated for users who experienced liver failure, cirrhosis progression, transplant, or death after taking the drug, alleging that Intercept Pharmaceuticals failed to warn about the risk of dosing toxicity and accelerated liver damage.
Roblox Lawsuit Families are filing Roblox lawsuits after children were targeted by predators for grooming, sextortion, sexual abuse, or exploitation on the platform. Learn who qualifies, what cases allege, and how to file a confidential claim.
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.
Bacterial Infection Outbreak at Nursing Homes and Hospitals Linked To Contaminated Syringes November 17, 2016 Russell Maas Add Your Comments Nursing home residents and hospital patients in at least five states have become infected with a specific strain of bacterium linked to a saline solution recall announced by federal health officials last month, resulting in several hospitalizations and potentially contributing to the death of at least six individuals. The U.S. Centers for Disease Control and Prevention (CDC) issued an update this week on a multistate outbreak of Burkholderia cepacia bloodstream infections, which have infected at least 151 individuals at 58 nursing homes and medical centers nationwide. The outbreak is linked to a Nurse Assist prefilled saline flush syringe recall announced last month by the FDA. Do You Know about… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know About… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION New Jersey has been the hardest hit by the outbreak. According to local news sources and the CDC, at least 13 new cases across New Jersey’s Atlantic County and Ocean County have been reported since the recall, bringing the state’s total of infected patients to 52. Investigations by health officials have revealed that many long-term care or nursing home facilities used the contaminated saline solution syringes prior to the recall. Currently, Maryland, New York, Delaware, Pennsylvania and New Jersey all have confirmed cases of B. Cepacia believed to be linked to the syringes. The recall involved syringes that are prepackaged saline flushes used in a healthcare setting to administer intravenous treatments, clearing central or arterial lines of any medicine or perishable liquids that could pose a sterilization hazard. Manufacturing company Nurse Assist Inc., in conjunction with the FDA, recalled any and all unexpired lots of the Nurse Assist I.V. Flush Syringe products that were distributed to customers and distributors between February 16, 2016 and September 30, 2016. The recalled products were sold in 3ml sizes with Product Code 1203, 5ml sizes with Product Code 1205, 10ml sizes with Product Code 1210, and 10ml sizes with Product Code 1210-BP. Product Numbers 1203, 1205, and 1210 were packaged 30 syringes to an inner carton and six inner cartons in a case totaling 180 syringes. Product Number 1210-BP was packaged with 400 syringes to a case. Burkholderia cepacia is a group of complex bacteria that can be found in soil and water and is often resistant to many common antibiotics, posing an increased risk to those with weakened immune systems such as children and the elderly. Although the bacterial infection poses no significant threat to healthy individuals, those with respiratory infections, specifically cystic fibrosis and chronic lung disease may be more susceptible to the bacteria and require immediate medical treatment. Common symptoms of the bloodstream infection include fevers, chills, clammy skin, shortness of breath, and abnormal heart rates among other side effects. Healthcare facilities known to have received and administered the recalled saline solutions to patients are being asked to monitor patients for side effects. Written by: Russell Maas Managing Editor & Senior Legal Journalist Russell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nation’s leading personal injury law firms and oversees the site’s editorial strategy, including SEO and content development. Tags: Burkholderia Cepacia, Hospital Infection, Infection, Medical Device Recall, Nursing Home, Syringe More Lawsuit Stories Internal Bra Side Effects Raise Questions About Manufacturers’ Knowledge of Mesh Failures October 27, 2025 Similac Lawsuit Claims Infant Formula Side Effects Led to Preemie’s Death October 27, 2025 Information About 2,500 Camp Lejeune Injury Claims May Influence Settlement Process October 27, 2025 0 Comments LinkedInThis 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 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 Term Δ MORE TOP STORIES Internal Bra Side Effects Raise Questions About Manufacturers’ Knowledge of Mesh Failures (Posted: today) Breast mesh products marketed as “internal bras” for lift and augmentation surgeries are now under investigation amid reports of painful complications, and questions over manufacturers’ prior knowledge of mesh-related risks. 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Internal Bra Side Effects Raise Questions About Manufacturers’ Knowledge of Mesh Failures October 27, 2025
Internal Bra Side Effects Raise Questions About Manufacturers’ Knowledge of Mesh Failures (Posted: today) Breast mesh products marketed as “internal bras” for lift and augmentation surgeries are now under investigation amid reports of painful complications, and questions over manufacturers’ prior knowledge of mesh-related risks. MORE ABOUT: BREAST MESH LAWSUITBreast Mesh Problems Prompted FDA Warnings Over Off-Label Use (10/15/2025)Breast Mesh Lawsuits May Follow Recent Studies Highlighting Internal Bra Complications (10/09/2025)FDA Warns BD Surgical Mesh Products Not Proven Safe for Breast Reconstruction Surgery (11/10/2023)
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