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.
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.
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.
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.
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.
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.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
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.
Similac Necrotizing Enterocolitis (NEC) Lawsuit Allowed To Proceed, With Certification Of Certain Claims to Conn. Surpeme Court Lawsuit alleges NEC resulted from Similac Neosure, Similac Human Milk Fortifier and Similac Special Car fed to premature baby in NICU August 23, 2021 Irvin Jackson Add Your Comments A federal judge has rejected an attempt by Abbott Laboratories to entirely dismiss a wrongful death lawsuit brought by the family of an infant that allegedly developed necrotizing enterocolitis (NEC) from Similac baby formula used in a hospital NICU, allowing certain claims to move forward and certifying other questions of law to the Connecticut Supreme Court. The original complaint (PDF) was brought by the family of Aries Peterson in the U.S. District Court for the Northern District of Connecticut in October 2020, presenting claims against Abbott for failure to warn, design defects, negligence, negligent misrepresentation, breach of express warranty, intentional misrepresentation, violations of the Connecticut Unfair Trade Practices Act (CUTPA) and loss of filial consortium under common law. Peterson was born prematurely and died after spending his entire three-month life in the neonatal intensive care unit (NICU) at Yale New Haven Hospital, in Connecticut. According to the family, the child died in April 2018, after developing NEC from Similac Neosure, Similac Human Milk Fortifier and Similac Special Care fed while hospitalized, each of which are cow’s milk-based products. Necrotizing enterocolitis (NEC) is a severe intestinal disorder among infants, which results in inflammation and necrosis of intestinal tissue. It primarily occurs among premature infants, and often results in death or devastating injuries. Over the last decade, a number of studies have indicated that use of cow’s milk baby formula like Similac and Enfamil may increase the risk of NEC in preterm infants. This has lead to a growing number of health experts recommending that premature babies only receive the mother’s breast milk, donor breast milk or certain breast-milk based formulas. Abbott Laboratories and Mead Johnson now face a growing number of Similac and Enfamil NEC lawsuits, alleging that they knew their products were unreasonably dangerous for premature babies, yet continued to sell and distribute the cow’s milk formula without providing adequate warnings to parents, hospitals and medical providers. In response to the complaint filed by the family of Aries Peterson, Abbott filed a motion to dismiss the complaint nearly in its entirety, and also asked the Court to strike allegations that it maintained were scandalous and inflammatory. In a 41-page opinion (PDF) issued on August 19, U.S. District Judge Stefan Underhill did agree to dismiss certain claims for negligent misrepresentation, intentional misrepresentation, breach of express warranty and violations of the CUTPA. However, the court allowed other claims to survive, including state law theories of failure to warn, design defect and negligence, as well as the parent’s claims for loss of filial consortium. BABY FORMULA NEC LAWSUITS Was your premature child fed Similac or Enfamil? Premature infants fed Similac or Enfamil cow’s milk formula face an increased risk of necrotizing enterocolitis (NEC) or wrongful death. Learn More SEE IF YOU QUALIFY FOR COMPENSATION BABY FORMULA NEC LAWSUITS Was your premature child fed Similac or Enfamil? Premature infants fed Similac or Enfamil cow’s milk formula face an increased risk of necrotizing enterocolitis (NEC) or wrongful death. Learn More SEE IF YOU QUALIFY FOR COMPENSATION In response to Abbott’s request to strike certain paragraphs from the complaint which asserted the company sought to profit by intentionally harming infants, plaintiffs’ argued that the allegations were substantive and relevant to Abbott’s potential recklessness. The Court denied that motion to strike, because “the allegations that Abbott argues are scandalous are really not.” Judge Underhill did indicate two questions of state law on those remaining claims will be certified to the Connecticut Supreme Court, including questions about whether the learned intermediary doctrine applies to the state law failure to warn theory and whether Connecticut law recognizes a cause of action for filial consortium, involving a parents claim for loss of a child’s affection, love and companionship. The parties have been directed to file either a stipulated statement of facts for the certification that will be filed to the Connecticut Supreme Court, or a written notice that they can not agree on such a stipulated statement, by September 20, 2021. Written by: Irvin Jackson Senior Legal Journalist & Contributing Editor Irvin 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: Abbott Laboratories, Infant Death, Necrotizing Enterocolitis, Similac, Wrongful Death Lawsuit Find Out If You Qualify for Infant Formula NEC Compensation More Baby Formula Lawsuit Stories Second NEC Baby Formula Bellwether Trial Will Not Move Forward July 29, 2025 Similac NEC Settlement Talks Result in MDL Census Order for Filed and Unfiled Claims July 24, 2025 Mead Johnson Must Face Enfamil NEC Lawsuit in Missouri State Court July 8, 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 TermLinkedInThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Dupixent T-Cell Lymphoma Lawsuits May Follow Recent Studies Linking Drug to Cancer Risks (Posted: today) Dupixent lawsuits are now being investigated after studies and FDA reports link Dupixent (dupilumab) to cutaneous T-cell lymphoma (CTCL). MORE ABOUT: DUPIXENT LAWSUITDupixent Side Effects May Increase Cutaneous T-Cell Lymphoma (CTCL) Risks (08/26/2025) Depo-Provera Meningioma Side Effects Significantly Increased Among Women Over 31: Study (Posted: yesterday) A new study appears to further confirm and quantify the risks of Depo-Provera meningioma side effects, potentially providing further evidence for growing litigation. 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