Rodriguez v. Abbott Laboratories

Appellate Court of Illinois·Decided September 11, 2026·No. 1-25-0423·Unpublished

Opinion

2026 IL App (1st) 250423-U FIRST DISTRICT,

SIXTH DIVISION

September 11, 2026

No. 1-25-0423

NOTICE: This order was filed under Supreme Court Rule 23 and is not precedent except in the limited circumstances allowed under Rule 23(e)(1).

IN THE

APPELLATE COURT OF ILLINOIS FIRST JUDICIAL DISTRICT

LUCINDA MARIA ALONSO RODRIGUEZ, )

Appeal from the

individually and as personal representative of the )

Circuit Court of

Estate of TRISTAN M. RODRIGUEZ, )

Cook County, Illinois.

)

Plaintiff-Appellee, )

No. 24 L 5821

v. )

)

Honorable

ABBOTT LABORATORIES, )

Brendan O’Brien,

)

Judge Presiding.

Defendant-Appellant. )

PRESIDING JUSTICE GAMRATH delivered the judgment of the court.

Justices Hyman and C.A. Walker concurred in the judgment.

ORDER

¶1 Held: Trial court abused its discretion in denying motion to dismiss based on forum non conveniens where private and public interest factors strongly favored dismissal.

¶2 On January 27, 2022, Tristan Rodriguez (Tris) was born in Florida at 27 weeks and 4 days’ gestation. In the Newborn Infant Care Unit (NICU) of Mount Sinai Medical Center in Florida, he was fed Similac, a cow’s-milk-based infant fortifier designed and distributed by

defendant Abbott Laboratories. On February 25, he was diagnosed with necrotizing enterocolitis (NEC), a deadly intestinal condition. He was transported for emergency treatment to Nicklaus Children’s Hospital in Florida and died in Florida on March 4.

¶3 His mother Lucinda Rodriguez (Lucinda), a resident of Florida, filed a product liability suit against Abbott in the circuit court of Cook County, Illinois. She alleged Similac consumption caused Tris’ NEC and eventual death, raising claims of defective design, failure to warn, and misrepresentation. Hundreds of similar suits alleging that cow’s-milk-based formula caused infants to develop NEC have been filed around the country, including a sizable number in Cook County.

¶4 Abbott filed a forum non conveniens motion to dismiss the case in favor of Florida. Although Abbott’s headquarters are in Lake County, Illinois, the business unit that makes and sells specialized infant formula products is in Ohio. Abbott presented the affidavit of Robyn Spilker, senior brand manager for health care provider marketing, who avers that the “vast majority” of Abbott employees with knowledge about research, design, development, sourcing, manufacture, packaging, sale, distribution, marketing, and promotion of Similac formula are in Ohio. Spilker identified 16 Abbott employees with information most likely to be relevant to the litigation, of which 15 are in Ohio, with the remaining one in Illinois.

¶5 Abbott also pointed out that all decisions relating to Tris’ nutrition were made in Florida and that testimony from Tris’ NICU medical team would be “critical.” In discovery, Lucinda identified 10 healthcare practitioners who provided treatment to Tris and one who provided treatment to herself relevant to the action. All 11 have business and/or residential addresses in Florida.

¶6 Abbott’s forum non conveniens motion was denied, and we granted Abbott’s petition for leave to appeal pursuant to Supreme Court Rule 306(a)(2) (eff. Oct. 1, 2020). After considering the totality of the circumstances and all relevant private and public interest factors, we find Abbott has proven the balance of factors strongly favors dismissal and, therefore, we reverse and remand with directions.

¶7 I. ANALYSIS ¶8 Forum non conveniens is an equitable doctrine allowing a court to decline jurisdiction if it appears another forum with proper venue “can better serve the convenience of the parties and the ends of justice.” Fennell v. Illinois Central R.R. Co., 2012 IL 113812, ¶ 12. For interstate forum non conveniens, our focus is “whether the case is being litigated in the most appropriate state.” Id. ¶ 13 (citing Eads v. Consolidated Rail Corp., 365 Ill. App. 3d 19, 25 (2006); 3 Richard A. Michael, Illinois Practice, Civil Procedure Before Trial § 14:1, 220 (2d ed. 2011)). The test is whether the relevant factors strongly favor dismissal in favor of the state proposed by the defendant. Id. ¶ 17. If so, the case will be dismissed, conditioned on the plaintiff timely filing the action in the other state and the defendant accepting service of process and waiving any statute of limitations defense. Id. ¶ 13.

¶9 Although plaintiff’s choice of forum is entitled to deference, that deference is less when neither her residence nor the site of the injury is in her chosen forum. First American Bank v. Guerine, 198 Ill. 2d 511, 517-18 (2002). Such is the case here.

¶ 10 When a defendant moves to dismiss on grounds of forum non conveniens, it bears the burden of showing plaintiff’s chosen forum is inconvenient to the defendant and another forum is more convenient to all parties. Fennell, 2012 IL 113812, ¶ 20. The court must evaluate the total circumstances of the case and balance the public and private interest factors in determining

whether they strongly favor dismissal. Id. ¶ 17. We review the circuit court’s ruling for an abuse of discretion, which occurs where no reasonable person would take the court’s view. Id. ¶ 21.

¶ 11 A. Private Interest Factors ¶ 12 Relevant private interest factors include: (a) the convenience of the parties; (b) the relative ease of access to sources of testimonial, documentary, and real evidence; (c) the cost of obtaining attendance of willing witnesses and the availability of compulsory process to secure attendance of unwilling witnesses; and (d) the possibility of viewing the premises, if appropriate. Id. ¶ 15.

¶ 13 Abbott’s primary contention is that access to testimony of third-party medical witnesses will be more convenient in Florida, where all decisions about Tris’ medical care were made and where all his treaters work. Lucinda urges us to give short shrift to this fact because this is a product liability case and “the forum non conveniens analysis should remain centered on product liability and not malpractice.” Had she alleged only a defective design, that point might carry weight. But by pleading multiple counts premised on failures to warn and deception of the medical professionals who treated Tris, she injects claims for which the location of those witnesses is plainly material.

¶ 14 We rejected a nearly identical argument by the plaintiffs in Deppa v. Abbott Laboratories, 2025 IL App (1st) 241795, a consolidated products liability suit in which plaintiffs alleged that infant formula caused their premature babies to develop NEC. As relevant here, Abbott filed a forum non conveniens motion seeking dismissal of 23 cases with infants who were born, injured, and treated in states other than Illinois. We found the location of the infants’ hospitals and doctors highly relevant:

“[P]laintiffs’ complaints focus not just on design defects and manufacturing of Abbott’s infant formula in Ohio. They zero in on Abbott’s sales and marketing of its formula to out-of-state hospitals and healthcare providers despite known dangers. The complaints allege that Abbott gave out-of-state hospitals, healthcare providers, and parents inadequate warnings and training about its formula. They allege that if the hospitals and healthcare providers had known of the risks associated with the formula, they would not have fed it to the injured infants. Plaintiffs also allege Abbott made misrepresentations to out-of-state hospitals and healthcare providers and used longstanding relationships to persuade them to provide the formula to these infants, causing serious injury or death.”

Id., ¶ 37.

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