Lawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms
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Court Urged to Establish Process for Selecting Baby Formula NEC Lawsuits For Bellwether TrialsA group of 12 baby formula NEC lawsuits will be selected for bellwether discovery, which will later be reduced down to four cases that will go before juries for the first federal trials. August 15, 2022 Irvin Jackson Add Your CommentsParties involved in baby formula NEC lawsuits being pursued against the makers of Similac and Enfamil have presented a plan to the U.S. District Judge presiding over the litigation, outlining the process for selecting a group of 12 cases that will be prepared for a series of early bellwether trials.Similac and Enfamil are cow’s milk infant formula products, which have been widely marketed in recent years to hospitals and families of new borns, including premature babies still in the NICU. However, increasing evidence has found that the baby formula greatly increase the risk of preemies developing a devastating gastrointestinal condition known as NEC, or necrotizing enterocolitis, which results in a painful destruction of the bowel.More than 100 families throughout the U.S. are now pursuing Similac NEC lawsuitย orย Enfamil NEC lawsuitย against Abbott Laboratories and Mead Johnson, alleging the manufacturers have known for years about the risks associated with use of their products among premature infants. However, as lawyers continue to review and file claims in the coming months and years, it is widely expected that the size of the litigation will increase dramatically, and will likely involve more 1,000 claims.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 COMPENSATIONGiven similar questions of fact and law raised in complaints filed in various different U.S. District Courts nationwide, the U.S. Judicial Panel on Multidistrict Litigation (JPML) established coordinated management for all NEC lawsuits against Similac and Enfamil manufacturers in April, requiring that any case filed throughout the federal court system be transferred to U.S. District Judge Rebecca R. Pallmeyer in the Northern District of Illinois for centralized discovery and pretrial proceedings.As part of the coordinated management of the NEC lawsuits, Judge Pallmeyer has indicated that a โbellwetherโ program will be established, where small groups of claims will go through case-specific discovery and early trial dates, to help gauge how juries are likely to respond to certain evidence that will be repeated throughout the litigation. However, if the parties fail to resolve the litigation during the MDL proceedings, each individual Similac and Enfamil case may later be returned to various different U.S. District Courts nationwide for separate trial dates.Proposed Baby Formula NEC Lawsuit Bellwether Selection PlanIn a proposed order (PDF) submitted on August 12, plaintiffs and defendants submitted a joint plan to Judge Pallmeyer, outlining how these first bellwether cases should be selected.According to the proposed plan, the cases would be chosen from those filed on or before September 16, 2022. By the end of next month, plaintiffs will provide the baby formula makers with a list of four initial bellwether discovery cases, no more than three of which can have Mead Johnson, the makers of Enfamil, as a defendant.On September 30, the parties will also provide the Court with a list of cases where Abbott, the maker of Similac, is the sole defendant, and a list where Mead Johnson is the sole defendant or a co-defendant with Abbott. They will then provide the court with a computer-generated application to randomly select four additional cases in total from those two lists.Finally, on or before November 23, 2022, the baby formula manufacturers will submit a list of four more cases, ensuring that the entire list of 12 potential bellwether trials has no more than five cases where Mead Johnson is a defendant.After fact discovery has been completed on the dozen initial bellwether discovery cases, each party will identify two cases to serve as initial bellwether trial cases, for a total of four claims that will be eligible to go before juries.The Court will later determine the order in which the cases will be tried, setting the cases about 12 weeks apart, according to the proposed plan.Although the outcome of these early bellwether trials will not have any binding impact on other claims, they are expected to have a substantial impact on any baby formula NEC settlements the manufacturers may offer to avoid the need for each individual case to be remanded back to U.S. District Courts nationwide for separate trial dates in the future. 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, Enfamil, Infant Death, Infant Formula, Mead Johnson, Necrotizing Enterocolitis, Preterm Birth, Similac Find Out If You Qualify for Infant Formula NEC CompensationMore Baby Formula Lawsuit Stories Enfamil NEC Lawsuit Cleared For MDL Trial in July 2026 May 14, 2026 Lawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms May 8, 2026 Mead Johnson Lawsuit Claims Premature Child Developed NEC From Enfamil April 24, 2026 0 Comments CommentsThis 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 Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: today)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: yesterday)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026) Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (Posted: 2 days ago)According to a man’s lawsuit, the failure of spinal cord stimulator device leads caused him to require revision surgery that resulted in heart problems and permanent health complications.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (05/19/2026)Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)
Lawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms May 8, 2026
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