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.
Epidemiologists Weigh Adding Cronobacter to Disease Watch List Following Similac Infant Formula RecallThe move to add cronobacter to a national disease watch list was sparked by last year’s Similac recall, which was linked to at least two infant deaths. May 11, 2023 Irvin Jackson Add Your CommentsFollowing a deadly Similac infant formula recall issued last year, which caused hundreds of reported illnesses nationwide, epidemiologists representing state health agencies will decide in June whether to recommend Cronobacter sakazaii be added to a list of diseases that must be reported to the federal government.The Council of State and Territorial Epidemiologists (CTSE) will vote on whether it will recommend the U.S. Centers for Disease Control and Prevention (CDC), which it partners with, add cronobacter to the National Notifiable Diseases Surveillance System. The list includes more than 100 illnesses of special priority due to their potential public health risks.Concerns about the widespread impact of cronobacter infections and illnesses gained nationwide attention last year, after Abbott Laboratories recalled Similac, Alimentum and Elecare formula productsย in February 2022, following the discovery of Cronobacter sakazakii and Salmonella Newport bacteria in powdered infant formula distributed nationwide, which has been blamed for at least two deaths.Similac Recall Over Cronobacter IllnessesThe infant formula recall was traced back to manufacturing problems at a Michigan facility, which was shut down after investigations revealed Abbott ignored industry safety standards and best practices at its facility for years, endangering children for the sake of profits.The cronobacter infections were widespread by the time the problems were reported to families nationwide. However, the manufacturer and health officials in at least some states were already aware of reports months before the recall was issued.Abbott now faces a number of Similac recall lawsuits and class action claims, alleging that it placed it’s desire for profits before the health and safety of children being fed their products.BABY FORMULA NEC LAWSUITSWas 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 MoreSEE IF YOU QUALIFY FOR COMPENSATIONBABY FORMULA NEC LAWSUITSWas 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 MoreSEE IF YOU QUALIFY FOR COMPENSATIONThe CTSE, which includes epidemiologists working with state and territorial health agencies throughout the U.S., has already identified cronobacter as a problem that requires closer investigation, and formed a working group during the winter to examine the problem. It is widely expected that the council will vote in June to add cronobacter to the national disease watchlist.If that occurs, it will call for all cases of cronobacter detected in the U.S. to be reported to the CDC. This could help the agency identify cronobacter outbreaks faster in the future, and help the CDC learn more about the illness itself, how it spreads, and could help prevent future outbreaks.Another major concern regarding cronobacter is that it is often misdiagnosed as sepsis or meningitis. A cronobacter misdiagnosis could result in poor treatment of the illness and could result in burgeoning outbreaks being missed in their early stages.Only two states currently require doctors report cronobacter cases, including Michigan and Minnesota.May 2023 Similac Recall Lawsuit UpdateProblems with Similac formula have resulted in two separate coordinated proceedings in the federal court system, including one multidistrict litigation (MDL) established before U.S. District Judge Matthew F. Kennelly in the Northern District of Illinois for all Similac, Alimentum and EleCare recall lawsuits. A separate MDL proceeding has also been established for all Similac lawsuitsย andย Enfamil lawsuitsย brought over the risk of necrotizing entercolotis (NEC) caused by cowโs milk formula products, which are centralized before U.S. District Judge Rebecca R. Pallmeyer.While early pretrial proceedings before Judge Kennelly areย still being established in the litigation over contaminated baby formula, Several Similac NEC lawsuits before Judge Pallmeyer have been selected for bellwether trials, which will be held to help the parties evaluate how juries will respond to certain evidence and testimony about the risks associated with use of cowโs milk formula among premature infants, which has been linked to NEC.Although the outcome of these bellwether trials will not be binding on other plaintiffs pursuing lawsuits against Abbott, they may have a large impact on the amount of Similac settlements the manufacturer may pay to avoid the need for each individual lawsuit to go before a separate jury. 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: Abbott Laboratories, Baby Formula Recall, Class Action Lawsuit, Cronobacter, Gastrointenstinal, Infant Formula, Infections, Necrotizing Enterocolitis, Salmonella, Similac, Similac Recall Find Out If You Qualify for Infant Formula NEC CompensationMore Baby Formula Lawsuit Stories Premature Infant Formula Lawsuit Alleges Enfamil Caused Necrotizing Enterocolitis (NEC) July 1, 2026 New Trial Ordered in Enfamil Lawsuit Over NEC Diagnosis June 22, 2026 EnfaCare Preterm Infant NEC Lawsuit Alleges Formula Caused Life-Threatening Diagnosis June 16, 2026 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 Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (Posted: today)A Boston Scientific spinal cord stimulator lawsuit claims the chronic pain implants are defectively designed, causing a Louisiana woman to suffer shocks and pain, as well as dizziness and fainting spells.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Lawsuits Warrant Centralization in New MDL: Motion (07/08/2026)Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026) First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (Posted: 3 days ago)The first Covidien hernia mesh bellwether trial begins on Monday in Massachusetts federal court involving claims that the Symbotex mesh is defectively designed.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (06/10/2026)Bard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026) Suboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (Posted: 4 days ago)Indivior faces nearly 18,000 Suboxone dental erosion lawsuits filed by individuals nationwide who say the opioid addiction treatment caused severe tooth damage.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)
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