Abbott Laboratories has agreed to a $670 million settlement to resolve claims from approximately 2,000 individuals alleging harm from the company's specialty formulas for preterm infants. The settlement includes a prior jury award of $495 million.

The settlement resolves a significant portion of the litigation against Abbott concerning alleged harm from its infant formulas, providing closure for many claimants and impacting the company's financial outlook.
Abbott Laboratories has agreed to a $670 million settlement to resolve legal claims from approximately 2,000 individuals who alleged harm related to the company's specialty formulas for preterm infants. The settlement includes a significant prior jury award of $495 million, where a jury found Abbott's infant formula caused necrotizing enterocolitis, a dangerous bowel disease, in an Illinois girl.
Abbott had been appealing the 2024 verdict to Missouri's Supreme Court. The company, which manufactures Similac formulas, faces similar lawsuits alongside Mead Johnson, a unit of Reckitt that produces Enfamil formulas. About 1,000 similar lawsuits have been filed, with over 800 cases centralized in an Illinois federal court and others pending in state courts across Illinois, Missouri, and Pennsylvania.
Necrotizing enterocolitis primarily affects premature newborns, leading to bowel tissue death and carrying a mortality rate exceeding 20%. Companies like Abbott and Mead Johnson have stated that while breast milk offers protection against the disease, their formulas do not cause it, and the benefits of breast milk have long been recognized by clinicians.
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