R.J. v. Mead Johnson & Company, LLC

District Court, N.D. Illinois·Decided December 8, 2023·No. 1:22-cv-02011·Unknown

Opinion

UNITED STATES DISTRICT COURT NORTHERN DISTRICT OF ILLINOIS EASTERN DIVISION

IN RE: ABBOTT LABORATORIES, et al., ) PRETERM INFANT NUTRITION PRODUCTS ) MDL No. 3026 LIABILITY LITIGATION ) _____________________________________ ) Master Docket No. 22 C 71 ) This Document Relates To: ) ) R.J., a minor, by his next of friend, ) Rebecca Donaldson, and Rebecca ) Donaldson, individually, ) ) Plaintiffs, ) ) v. ) No. 22 C 2011 ) MEAD JOHNSON & COMPANY, LLC, ) Judge Rebecca R. Pallmeyer et al., ) ) Defendants. )

MEMORANDUM OPINION AND ORDER This case is one of hundreds consolidated by the Judicial Panel on Multidistrict Litigation (“JPML”) and pending before this court, in which plaintiffs have alleged that infant formula manufactured by defendants caused necrotizing enterocolitis (“NEC”) in babies born prematurely. Plaintiff Rebecca Donaldson and Donaldson’s minor child, R.J., filed this case in the Western District of Missouri against one of the manufacturers, Mead Johnson & Company, LLC and Mead Johnson Nutrition Company; the parties are of diverse citizenship. Earlier this year, the court issued a Memorandum Opinion and Order [26], concluding that Mead Johnson was subject to general jurisdiction in Missouri by virtue of that state’s corporate registration statute. Mead Johnson has moved for reconsideration of that aspect of the court’s ruling and, for the reasons noted here, the court grants that motion and vacates Section I of its prior order. Because no other basis exists for the Missouri district court to exercise personal jurisdiction over Mead Johnson, the court dismisses this action without prejudice to refiling in Kansas or, if the parties agree, directly in this court. BACKGROUND I. Factual Background The court reviewed the facts in its earlier opinion but revisits them here. Plaintiff Rebecca Donaldson, a resident of Missouri, gave birth to her son, R.J., at Overland Hospital (“Overland”), in Overland Park, Kansas, on February 20, 2010. (Pl.’s First Am. Compl. (“Am. Compl.”) [14] ¶ 34.) Overland is less than ten miles from the Missouri border. (Id. ¶¶ 7–8, 34.) R.J. was premature, arriving at 31 weeks’ gestational age; he weighed only 1540 grams (just under three and a half pounds). (Id. ¶ 34.) After a week in Overland’s NICU, doctors started R.J. on “low- volume feeds by mouth” of Mead Johnson’s infant formula, Enfamil Premature Infant Formula 24 Calories with Iron. (Id. ¶¶ 9, 35.) By March 5, R.J. began exhibiting serious symptoms of NEC, including “distended loops of bowel and bloody stool” and gas building up within his intestinal walls. Doctors diagnosed R.J. as suffering from NEC, stopped feeding him Enfamil, and started him on antibiotics. (Id. ¶ 36.) On March 7, R.J. was transported from Overland Hospital to the University of Kansas Medical Center, where he stayed for months, undergoing numerous surgeries—including three “exploratory laparotom[ies]”—to remove large swaths of necrotized bowel tissue from his gastrointestinal tract. (Id. ¶¶ 37–40.) Every day during that period, R.J.’s mother drove the fifteen- minute trip from her Missouri home to see him. (Id. ¶ 40.) He was finally released from the hospital on June 12, 2010, 112 days after his premature birth, and has “continually resided in Missouri” since then, undergoing treatment in Kansas City, Missouri to the present day to confront a devastating host of symptoms, including “constant diarrhea” and “short gut syndrome.” (Id. ¶¶ 40–41.) Mead Johnson manufactures and distributes Enfamil, its infant formula, in every state, including Missouri. (Id. ¶ 9.) Mead Johnson is incorporated in Delaware and its principal place of business “has been located in Illinois and/or Indiana,”1 but it also “registered [to do business] with the Missouri Secretary of State” in February of 2010 and December of 2012. (Id. ¶¶ 9–10.) From 2008 until 2020, Mead “held an exclusive contract” in Missouri for the “Special Supplemental Nutrition Program for Women, Infants, and Children” (“WIC”), a federal program providing nutritional assistance and social services to low-income mothers and others. Sales pursuant to that contract formed “an important part of [Mead’s] U.S. Business . . . .” (Id. (quoting Form S-1 Registration Statement Under the Securities Act of 1933: Mead Johnson Nutrition Company (2008), https://www.sec.gov/Archives/edgar/data/1444904/000119312508196083/ds1.htm.) According to Plaintiffs, Mead also employs “numerous key opinion leaders and employees” in Missouri, at least some of whom “engage in significant outreach” from Missouri to Kansas City doctors. (Am. Compl. ¶ 11.) Plaintiffs further allege that Mead maintains “investigator sites” related to its formula in Missouri, and that its parent company “maintains a logistical center” in St. Peters, Missouri.2 (Id.) Finally, Plaintiffs allege that Mead’s misleading marketing led Ms. Donaldson to “belie[ve] that Defendant’s products were safe for Baby R.J.,” and that “R.J.’s Mother and physicians would not have fed Baby R.J. Defendants’ Cow’s Milk-Based Products if she/they had known of the extreme risk to her child” they posed. (Id. ¶¶ 29–32.) II. Procedural Background More than a decade after R.J.’s birth, on March 4, 2022, Plaintiffs sued Mead Johnson in the Western District of Missouri, alleging that ingesting Mead’s cow’s-milk-based infant formula or infant milk fortifiers made from cow’s milk caused R.J.’s NEC. (Compl. [1] at 1–2.) On January 31, 2023, Mead Johnson moved to dismiss Plaintiffs’ claim on multiple grounds. First, Mead

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