Active LitigationMDL 3026
Toxic Baby Formula NEC Lawsuit Facts
TorHoerman Law is actively accepting claims for the Toxic Baby Formula NEC Lawsuit.
Active Litigation·MDL 3026
TorHoerman Law is actively accepting claims for the Toxic Baby Formula NEC Lawsuit.
NEC baby formula lawsuits remain active in federal multidistrict litigation and state courts.
The litigation involves claims against Abbott Laboratories, the manufacturer of Similac, and Mead Johnson, the manufacturer of Enfamil, over allegations concerning cow’s milk-based formulas and the risk of necrotizing enterocolitis (NEC) in premature infants.
Abbott has separately reached agreements resolving a significant number of Similac NEC claims, while litigation involving Mead Johnson and Enfamil continues.
TorHoerman Law is no longer accepting NEC clients with claims against Similac. We are still accepting clients with claims against Enfamil.

There is currently no global settlement resolving all NEC baby formula lawsuits.
Federal cases remain consolidated in MDL No. 3026 in the U.S. District Court for the Northern District of Illinois, while separate NEC lawsuits continue in state courts.
Abbott Laboratories has reached agreements resolving the Gill case and claims involving approximately 2,000 additional individuals with NEC claims involving its specialty formulas for premature infants.
Those agreements concern Abbott and do not resolve NEC claims involving Mead Johnson or Enfamil.
Cases involving Mead Johnson continue to proceed through the courts, and no global Enfamil NEC settlement has been announced.
TorHoerman Law is no longer accepting NEC clients with claims against Similac.
We are still accepting clients with claims against Enfamil.
If your child developed NEC after receiving an Enfamil cow’s milk-based formula or fortifier in a hospital or NICU, contact our law firm for a free consultation or use the chatbot on this page to request a free case review.
The NEC Baby Formula Lawsuit refers to a significant amount of cases filed against major baby formula manufacturers, specifically Abbott Laboratories (maker of Similac Infant Formula) and Mead Johnson & Company (maker of Enfamil Formula).
Infant Formula NEC Lawsuits claim that premature babies fed cow milk based formulas are at an increased risk to develop NEC.
Scientific studies have shown that premature infants fed cow milk based formula were at an increased risk to develop NEC compared to premature infants fed only human breast milk.
Enfamil and Similac Baby Formula Lawsuits allege that the manufacturers failed to adequately warn healthcare providers and parents about the potential dangers associated with their products, despite knowing the risks involved.

Families pursuing NEC lawsuits may seek compensation for medical expenses, long-term care, pain and suffering, and other losses associated with the child’s injuries.
The damages available in an individual case depend on the facts of the claim and applicable law.
NEC baby formula litigation continues in federal and state courts, with recent cases producing different outcomes.
TorHoerman Law obtained a $495 million jury verdict against Abbott Laboratories in July 2024.
The Missouri Court of Appeals affirmed that verdict in May 2026.
In August 2026, Abbott announced agreements resolving the Gill case and NEC claims involving approximately 2,000 additional individuals for an aggregate amount of approximately $670 million.
Litigation involving Mead Johnson has followed a different course.
A $60 million Illinois verdict against Mead Johnson was reversed on appeal and returned to the trial court for further proceedings.
In August 2026, a federal jury returned a defense verdict for Mead Johnson in the Inman case, the first Mead Johnson bellwether in the federal NEC multidistrict litigation to reach a jury.
These results show that NEC lawsuits remain highly dependent on the medical evidence, feeding history, warnings at issue, applicable law, and circumstances of each individual case.
No global settlement has been announced for Enfamil NEC claims.
The NEC Baby Formula Lawsuits are centered around claims that major baby formula manufacturers, such as Abbott Laboratories (maker of Similac) and Mead Johnson & Company (maker of Enfamil), knowingly marketed and sold cow’s milk-based formulas that significantly increased the risk of necrotizing enterocolitis (NEC) in premature infants and low birth weight babies.
NEC Baby Formula Plaintiffs argue that these companies failed to adequately warn parents and healthcare providers about the heightened risks associated with their products, despite mounting scientific evidence linking cow’s milk-based formulas to NEC.
Legal claims in the NEC Infant Formula Litigation typically include product liability, negligence, failure to warn, and breach of warranty, among other potential claims.
The companies have generally responded by denying the allegations, arguing that their products are safe and that NEC is a multifactorial condition with no definitive link to formula feeding.
They have also asserted that they provided sufficient warnings and that the benefits of their products outweigh the risks.

Plaintiffs allege that evidence developed during the litigation supports their claims that formula manufacturers knew about concerns surrounding NEC risk in premature infants but failed to provide adequate warnings.
Abbott Laboratories and Mead Johnson dispute the allegations and have defended the safety and medical use of their preterm nutrition products.
The outcome of an individual NEC lawsuit depends on the evidence and legal issues presented in that particular case.
Necrotizing enterocolitis (NEC) is a severe gastrointestinal condition that primarily affects premature infants, especially those born before 37 weeks of gestation.
The disease causes inflammation and bacterial invasion of the intestinal wall, leading to the death of intestinal tissue and, in severe cases, perforation of the bowel.
This perforation allows harmful bacteria to leak into the abdomen, potentially leading to widespread infection and sepsis, which can be life-threatening.
The exact cause of NEC is not fully understood, but it is believed to involve a combination of factors, including an immature immune system, reduced blood flow to the intestines, and the introduction of bacteria through feeding, particularly when cow’s milk-based formulas are used.
NEC can develop rapidly and requires immediate medical attention.
Symptoms often include feeding intolerance, abdominal swelling, bloody stools, and lethargy.
Despite advances in neonatal care, NEC remains one of the leading causes of illness and death in preterm infants.
Treatment typically involves stopping feedings, draining the stomach, administering antibiotics, and, in severe cases, surgery to remove the damaged portion of the intestines.
Even with prompt treatment, many infants who survive NEC face long-term complications that can significantly impact their quality of life.

Complications of necrotizing enterocolitis (NEC) include:
Cow’s milk-based baby formulas, such as Similac and Enfamil, have been linked to an increased risk of developing necrotizing enterocolitis (NEC) in premature infants.
Research has shown that preterm infants who are fed cow’s milk-based formulas are more likely to develop NEC compared to those who are exclusively fed human milk.
The immature intestines of premature babies are less capable of digesting cow’s milk proteins, which can lead to inflammation, bacterial overgrowth, and eventually, NEC.
A meta-analysis published in the journal Pediatrics found that preterm infants fed human milk were 77% less likely to develop NEC than those fed cow’s milk-based formula.
The Journal of Perinatology has highlighted that the introduction of cow’s milk-based formula into the diet of preterm infants disrupts the gut microbiota, increasing the likelihood of intestinal inflammation.
Despite these findings, many hospitals continue to use cow milk formulas in neonatal intensive care units (NICUs) due to their availability and cost, which raises ethical concerns about patient safety versus profitability.
These scientific insights are central to the ongoing lawsuits against formula manufacturers, as plaintiffs argue that the companies failed to adequately warn about these known risks.
Medical research comparing human milk and cow’s milk-based nutrition in premature infants has become an important part of the scientific evidence cited in NEC baby formula litigation.
The NEC Baby Formula Lawsuits specifically target certain Similac and Enfamil formula products that are alleged to increase the risk of necrotizing enterocolitis (NEC) in premature infants.
NEC Lawsuits claim that these cow’s milk-based formulas were marketed and used in hospitals despite evidence of their potential dangers to vulnerable infants.
Similac Infant Formulas Named in NEC Lawsuits:
Enfamil Baby Formula Products Named in NEC Lawsuits:
Lawsuits naming Similac and Enfamil premature infant formula are specifically for the types of infant formulas used in hospitals and medically administered by healthcare professionals.
Similac and Enfamil formula sold on the shelves of supermarkets and stores across the country are separate products and are not included in the NEC Baby Formula Lawsuits.
The specific type of infant formulas used in the NICU will likely be listed on the medical and feeding records related to the treatment of your premature baby.
TorHoerman Law is currently accepting potential NEC claims involving Enfamil products manufactured by Mead Johnson.
A family may qualify for an Enfamil NEC case review when a premature or low-birth-weight infant received an Enfamil cow’s milk-based formula or fortifier in a hospital or neonatal intensive care unit (NICU) and was later diagnosed with necrotizing enterocolitis.
Relevant factors may include:
TorHoerman Law is no longer accepting NEC clients with claims against Similac. We are still accepting clients with claims against Enfamil.
Contact our law firm for a free consultation or use the chatbot on this page to find out whether you may qualify for an Enfamil NEC claim.
Medical and hospital records may provide important evidence about a premature infant’s formula exposure, NEC diagnosis, treatment, and resulting injuries.
Evidence relevant to an Enfamil NEC claim may include:
These records may help establish the product administered, the timing of exposure and diagnosis, and the medical consequences associated with the child’s NEC.
Damages in an NEC lawsuit refer to economic and non-economic losses allegedly resulting from the child’s injuries.
The types and amount of damages available depend on the severity of the child’s condition, medical treatment, long-term needs, applicable state law, and other circumstances of the individual claim.
Damages sought in NEC lawsuits may include:
The damages available in an individual NEC lawsuit depend on the evidence and law applicable to the claim.
The NEC Baby Formula Lawsuit refers to legal actions taken against major baby formula manufacturers, specifically Abbott Laboratories (maker of Similac) and Mead Johnson & Company (maker of Enfamil).
NEC Infant Formula Lawsuits allege that the cow’s milk-based formulas manufactured by these companies significantly increase the risk of necrotizing enterocolitis (NEC) in premature infants.
NEC is a severe and potentially fatal gastrointestinal condition that primarily affects premature babies.
Plaintiffs argue that the manufacturers failed to provide adequate warnings about these risks, leading to devastating health outcomes for affected infants.
Baby Formula Lawsuits are being handled both in multidistrict litigation (MDL) in federal court and in various state courts across the United States.
Products from popular baby formula makers Abbott Laboratories and Mead Johnson are named in the NEC Baby Formula Lawsuits.
NEC Lawsuits specifically target medically administered cow’s milk-based formulas like Similac and Enfamil, which are not the typical products found on store shelves.
Instead, these formulas are specially designed for and administered to premature infants in hospital settings, often in neonatal intensive care units (NICUs).
They are used to meet the nutritional needs of preterm infants who require enhanced calories and protein for growth and development.
However, plaintiffs argue that these formulas significantly increase the risk of necrotizing enterocolitis (NEC) in these vulnerable infants and that the manufacturers failed to adequately warn about these risks.
As a result, families are seeking compensation for the harm caused by these products, claiming they were not properly informed of safer alternatives, such as human milk fortifiers.
Parents and legal guardians may be able to pursue an Enfamil NEC lawsuit when a premature infant received an Enfamil cow’s milk-based formula or fortifier in a hospital or NICU and was later diagnosed with necrotizing enterocolitis.
Medical and feeding records may help identify the Enfamil product administered, document the timing of the NEC diagnosis, and establish the injuries and treatment that followed.
A wrongful death claim may also be available under applicable state law when a child dies from complications associated with NEC.
TorHoerman Law is no longer accepting NEC clients with claims against Similac. We are still accepting clients with claims against Enfamil.
The time limit to file an NEC Baby Formula Lawsuit, known as the statute of limitations, varies by state and the specific circumstances of each case.
Generally, the statute of limitations for product liability lawsuits ranges from 2 to 3 years from the date of injury or the discovery of the injury’s cause.
However, in cases involving infants, some states may allow for extensions based on when the link between the formula and NEC was discovered or should have been discovered by the parents.
It’s crucial to consult with an attorney promptly to ensure that your claim is filed within the appropriate timeframe.
A Toxic Baby Formula Lawyer from TorHoerman Law can help analyze your case and inform you of the legal requirements for filing a NEC Lawsuit.
Families who file an NEC Baby Formula Lawsuit may be eligible to recover various types of compensation depending on the severity of the infant’s condition and the impact on the family’s life.
Compensation can include medical expenses for both past and future treatments, pain and suffering endured by the infant, and emotional distress experienced by the family.
In cases where the infant suffered long-term disabilities or died as a result of NEC, compensation could also cover loss of future earnings and funeral expenses.
Punitive damages may be awarded in cases where it is proven that the manufacturers acted with gross negligence or intentionally withheld critical safety information from consumers.
No, there is not a Baby Formula NEC Class Action Lawsuit.
Instead, the NEC Baby Formula lawsuits are being handled through a multidistrict litigation (MDL) process and individual state court filings.
Unlike a class action, where one lawsuit represents a large group of plaintiffs collectively, the MDL consolidates similar cases to streamline pretrial proceedings but keeps each case separate.
This allows for individualized consideration of the damages and circumstances of each case. Families affected by NEC can pursue their claims independently, which may result in more tailored compensation based on the specific details of their situation.

Tor Hoerman has represented injured individuals for more than 30 years, with experience spanning individual personal injury cases and nationwide mass tort litigation. His work includes car accidents, catastrophic injuries, product liability claims, and other serious injury cases. Tor has served in court-appointed leadership roles in national litigation and tried cases involving major corporate defendants.
TorHoerman Law’s legal content is researched and written by our editorial team and attorneys for legal accuracy, clarity, and relevance. We rely on statutes, court records, government publications, medical research, and other authoritative sources when applicable. This page provides general legal information and does not constitute legal advice.
TorHoerman Law reviews its legal content for factual accuracy, current information, and relevant legal context before publication and as material developments occur. This article is provided for general informational purposes and does not constitute legal advice. For guidance about a specific case, contact TorHoerman Law.
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