Harrell v. Abbott Laboratories

CourtDistrict Court, N.D. Illinois
DecidedAugust 29, 2022
Docket1:22-cv-03590
StatusUnknown

This text of Harrell v. Abbott Laboratories (Harrell v. Abbott Laboratories) is published on Counsel Stack Legal Research, covering District Court, N.D. Illinois primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Harrell v. Abbott Laboratories, (N.D. Ill. 2022).

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: ) Removed California Cases1 ) Judge Rebecca R. Pallmeyer )

MEMORANDUM OPINION AND ORDER In this opinion, the court addresses motions to remand in six related cases within the multidistrict litigation. Each case was filed in California state court, removed to federal court by Defendant Abbott Laboratories, and transferred to this district by the Judicial Panel on Multidistrict Litigation. Plaintiffs believe these cases should be remanded to state court for lack of federal subject-matter jurisdiction. Each Plaintiff, a California citizen, brings at least one claim against a California-based hospital—a fact that would appear to frustrate the requirement of complete diversity. Abbott nevertheless urges the court to disregard the nondiverse hospital defendants and retain these cases in the MDL. Citing the fraudulent joinder doctrine, Abbott contends that Plaintiffs do not state any viable claims against the hospital defendants, having joined them solely to frustrate diversity and avoid federal court. As explained below, the court concludes that Abbott has not met its heavy burden to establish fraudulent joinder and grants Plaintiffs’ motions to remand.

1 This opinion resolves motions to remand in six cases that were removed from California state court before being transferred to this district and consolidated in the MDL: Pariani v. Mead Johnson & Co., No. 22 C 4115 [8, 27]; Lafond v. Mead Johnson & Co., No. 22 C 4116 [7, 30]; Thomas v. Mead Johnson & Co., No. 22 C 4117 [11, 39]; Tracy v. Mead Johnson & Co., No. 22 C 4118 [14, 44]; Hartwick v. Mead Johnson & Co., No. 22 C 4120 [10, 43]; and Harrell v. Abbott Laboratories, No. 22 C 3590 [24]. BACKGROUND2 Each Plaintiff is a natural person and a citizen of California. (Compl. ¶¶ 3–10, Thomas, No. 22 C 4117 [1-2] (hereinafter “Compl.”).) Plaintiffs’ claims arise out of injuries suffered by their preterm infants, who were given cow’s-milk-based formula that allegedly caused the infants to develop a dangerous gastrointestinal condition called necrotizing enterocolitis (“NEC”). (Id. ¶ 1.) Plaintiffs assert claims against two sets of Defendants: the “Manufacturer Defendants” (including Abbott) and the “Hospital Defendants.”3 As their name implies, the Manufacturer Defendants manufacture and market cow’s-milk-based infant formula products. (Id. ¶¶ 11–12.) The Hospital Defendants own and operate the California hospitals where the injured infants were fed the Manufacturer Defendants’ products. (Id. ¶ 13.) Plaintiffs allege that “[e]xtensive scientific research” has confirmed that cow’s-milk-based formula products “cause NEC in preterm and low-birth-weight infants.” (Id. ¶ 50.) According to Plaintiffs, there exist several options for feeding preterm infants that are safer than cow’s-milk- based products, such as “the mother’s own milk,” “pasteurized donor breast milk” (which can be delivered nationwide through “an established network”), and “shelf-stable formula and fortifiers derived from pasteurized breast milk.” (Id. ¶ 58.)

2 For the factual background section, the court draws on the complaint in Thomas, No. 22 C 4117. Counsel representing Plaintiffs in five of these cases (all but Harrell) has averred that Thomas is representative of the other four in that group, at least with respect to the remand briefing. (See, e.g., Decl. of Alexandra M. Walsh ¶¶ 3–8, Pariani, No. 22 C 4115 [28].) The court has also reviewed the complaint in Harrell and concluded that it is materially identical for the purpose of this brief factual overview.

3 The Hospital Defendants are Northbay Healthcare Group d/b/a Northbay Medical Center (in Pariani, No. 22 C 4115); Dignity Health d/b/a Mercy Medical Center Redding (in Lafond, No. 22 C 4116); Sutter Bay Hospitals d/b/a Alta Bates Summit Medical Center Alta Bates Campus and Alta Bates Summit Medical Center Summit Campus (in Thomas, No. 22 C 4117); Regents of the University of California, Kaiser Foundation Hospitals d/b/a Kaiser Permanente Walnut Creek Medical Center, Kaiser Permanente Santa Rosa Medical Center, and Kaiser Permanente San Francisco Medical Center (in Tracy, No. 22 C 4118); Kaiser Foundation Hospitals Inc. d/b/a Kaiser Permanente Oakland Medical Center, Kaiser Permanente San Leandro Medical Center, and Kaiser Permanente Hayward Medical Center (in Hartwick, No. 22 C 4120); and Dignity Health d/b/a Mercy San Juan Medical Center (in Harrell, No. 22 C 3590). Plaintiffs allege that the relative dangers of cow’s-milk-based formula products were already well known when their infants were fed the Manufacturer Defendants’ products at the Hospital Defendants’ facilities. (Id. ¶ 62.) Based on this scientific evidence, Plaintiffs say, the Hospital Defendants “knew or should have known” that allowing the Manufacturer Defendants’ products to be given to Plaintiffs’ preterm infants would increase the infants’ risks of developing NEC. (Id. ¶ 90.) But the Hospital Defendants have allegedly “continued to purchase, supply, and distribute” the Defendant Manufacturers’ products in their hospitals “without providing full and adequate warnings of the attendant risks to parents, healthcare professionals, and other medical staff at its relevant facilities.” (Id. ¶ 94.) Plaintiffs bring several claims against the Manufacturer Defendants, including strict liability design defect, strict liability failure to warn, negligence, intentional misrepresentation, and negligent misrepresentation. (Id. ¶¶ 99–144.) As between Plaintiffs (who are domiciled in California) and the Manufacturer Defendants, there is diversity of citizenship: Defendant Mead Johnson Nutrition Company is incorporated in Delaware and has its principal place of business in either Illinois or Indiana (see id. ¶ 11; Notice of Removal ¶ 28, Thomas, No. 22 C 4117 [1]), Defendant Mead Johnson & Company, LLC is a limited liability company that is organized under the laws of Delaware and has the citizenship of its sole member, Mead Johnson Nutrition Company (Compl. ¶ 11), and Defendant Abbott is incorporated in and has its principal place of business in Illinois (id. ¶ 12). In addition to their claims against the Manufacturer Defendants, each Plaintiff brings a claim for negligent failure to warn against at least one Hospital Defendant.4 (Id. ¶¶ 145–58.) As

4 Some Plaintiffs have also brought survival and wrongful death claims against one or more Hospital Defendants. (See, e.g., Compl. ¶¶ 159–65.) Under California law, to recover for survival or wrongful death, the plaintiff must establish an underlying claim. See Lattimore v. Dickey, 239 Cal. App. 4th 959, 968, 191 Cal. Rptr. 3d 766, 773 (2015) (noting that a wrongful death action requires an underlying tort); Quiroz v. Seventh Ave. Ctr., 140 Cal. App. 4th 1256, 1264, 45 Cal. Rptr. 3d 222, 227 (2006) (noting that a survival action derives from a claim that the decedent possessed before their death). The court’s fraudulent joinder analysis therefore addresses only between Plaintiffs and these Defendants, diversity is lacking: Each Hospital Defendant is incorporated in and has its principal place of business in California, where Plaintiffs are domiciled. (Id. ¶ 13.) PROCEDURAL HISTORY Each of these six cases was filed in California state court by Plaintiffs, removed to federal court by Abbott, and transferred to this district by the Judicial Panel on Multidistrict Litigation. In one of the six cases, Harrell, Plaintiff did not file a motion to remand until after the case had been transferred to this district and consolidated in the MDL. The parties addressed their briefs on that motion directly to this court, relying on Seventh Circuit precedent on fraudulent joinder.

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Harrell v. Abbott Laboratories, Counsel Stack Legal Research, https://law.counselstack.com/opinion/harrell-v-abbott-laboratories-ilnd-2022.