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Mead Johnson wins jury verdict in lawsuit over preterm baby formula

Created at 2 Jul · 7:13 PM1 source↑ Market-relevant
IN SHORT

A Missouri jury rejected claims that Mead Johnson's specialized formula for preterm babies caused a dangerous bowel disease in an infant. The verdict sides with the Enfamil maker in a case brought by an Illinois mother, marking the latest trial in nearly 1,000 similar lawsuits.

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Key Numbers

1,000similar lawsuits filed against Enfamil and Similac makers
700cases centralized in an Illinois federal court
20%estimated mortality rate for necrotizing enterocolitis
$60 millionverdict previously reversed against Mead Johnson

Who's Involved

Mead Johnson
Enfamil maker, sided with by jury in lawsuit
Cadence Collins
Illinois mother who sued Mead Johnson
Reckitt
Parent company of Mead Johnson
Abbott Laboratories
Maker of Similac formulas, also facing similar lawsuits
Robert Ford
CEO of Abbott Laboratories
Mead Johnson wins jury verdict in lawsuit over preterm baby formula

↳ Why This Matters

The verdict is significant as it represents a key legal battleground in ongoing litigation against formula manufacturers concerning allegations that their products for premature infants cause necrotizing enterocolitis, potentially impacting future legal outcomes and the availability of these specialized nutritional products.

Key facts

  • A Missouri jury ruled in favor of Mead Johnson, maker of Enfamil, in a lawsuit alleging its specialized preterm baby formula caused necrotizing enterocolitis (NEC).
  • The lawsuit was filed by Cadence Collins, an Illinois mother whose infant daughter allegedly suffered lifelong injuries from the formula.
  • Mead Johnson, a unit of Reckitt, stated it strongly rejects any assertion that its specialized preterm hospital nutrition products cause NEC.
  • The case is one of nearly 1,000 similar lawsuits filed against Mead Johnson and Abbott Laboratories, which makes Similac formulas.
  • The products in question are cow's milk-based formula and fortifiers for mother's milk intended for hospital settings.

A jury in St. Louis has rejected claims that Mead Johnson's specialized formula for preterm babies was responsible for causing a dangerous bowel disease in an infant. The verdict on Thursday sided with the Reckitt unit, Mead Johnson, in a lawsuit brought by Illinois mother Cadence Collins. Collins had claimed her daughter suffered lifelong injuries after contracting necrotizing enterocolitis, a condition that primarily affects premature newborns and has a mortality rate exceeding 20%, as a result of consuming Mead Johnson's product.

The trial is one of nearly 1,000 similar lawsuits filed against both Mead Johnson and Abbott Laboratories, which produces Similac formulas. Over 700 of these cases are consolidated in an Illinois federal court, with others pending in state courts across Illinois, Missouri, and Pennsylvania.

Mead Johnson issued a statement asserting, "We strongly reject any assertion that any of our specialized preterm hospital nutrition products cause NEC." The companies maintain that while breast milk offers protection against the bowel disease, their formulas do not cause it, and the benefits of breast milk have long been recognized by clinicians.

Attorneys for Collins indicated they disagreed with the jury's decision and would explore all available options for their client. The products at the center of these lawsuits are cow's milk-based formulas and milk fortifiers designed for infants in hospital settings, not standard formulas sold to consumers.

In 2024, Abbott CEO Robert Ford suggested that litigation might lead to the discontinuation of these preterm products. The companies have experienced mixed results in trials so far, with some juries ruling in their favor and others siding with the parents. Last month, an Illinois appeals court overturned a $60 million verdict against Mead Johnson, citing improper jury instructions regarding claims that the company failed to warn about the potential for necrotizing enterocolitis from its premature baby products.

Frequently asked questions

Necrotizing enterocolitis is a serious intestinal disease that primarily affects premature newborns, causing the death of bowel tissue. It has an estimated mortality rate of over 20%.

There are nearly 1,000 similar lawsuits filed against the makers of Enfamil and Similac formulas, with over 700 centralized in an Illinois federal court.

Last month, an Illinois appeals court reversed a $60 million verdict against Mead Johnson in a case alleging failure to warn about NEC risks, stating the jury was not properly instructed on the law.

What Happens Next

01Attorneys for Cadence Collins will evaluate all legal options.
02Further trials are expected in similar lawsuits against Mead Johnson and Abbott Laboratories.

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Cadence

How It Developed

A jury in St. Louis rejected claims that Mead Johnson's specialized formula for preterm babies caused necrotizing enterocolitis.
The lawsuit was brought by an Illinois mother, Cadence Collins, who claimed her daughter suffered lifelong injuries.
Mead Johnson stated that its specialized preterm hospital nutrition products do not cause NEC.
The companies maintain that while breast milk protects against the disease, their formulas do not cause it.
Attorneys for Collins stated they would evaluate all options following the verdict.
An Illinois appeals court previously reversed a $60 million verdict against Mead Johnson in a similar case.

Sources

T1
Missouri jury sides with Enfamil maker Mead Johnson in case over preterm baby formulaReuters

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