Stephanie Foster, Sophie Capshaw-Mack, and Olga Otkina, et al. v. The Proctor & Gamble Company

District Court, N.D. Illinois·Decided July 15, 2026·No. 1:25-cv-09735·Unknown

Opinion

UNITED STATES DISTRICT COURT FOR THE NORTHERN DISTRICT OF ILLINOIS EASTERN DIVISION

STEPHANIE FOSTER, SOPHIE CAPSHAW-MACK, and OLGA OTKINA, et al., individually and on No. 25 CV 9735 behalf of all others similarly situated, Plaintiffs Judge Jeremy C. Daniel

v.

THE PROCTOR & GAMBLE COMPANY, Defendant.

ORDER The defendant’s motion to dismiss [48] is granted in part and denied in part. Specifically, it is granted as to the third cause of action, but it is denied as to all others. The defendant shall answer the complaint on or before July 31, 2026. The July 16, 2026, status hearing is stricken.

Background

This case is before the Court on defendant The Proctor & Gamble Company’s (“P&G”) motion to dismiss Plaintiffs Stephanie Foster, Sophie Capshaw-Mack, Olga Otkina, Amanda Murray, Einaya Morciglio, Carmuse Mitchem, Stephanie Maya, Wendy Rodriguez, Dena Habboush, Lareina Green, and Katherine Vescovo’s consolidated class action complaint (“CCAC”). (R. 48.) The facts below are drawn from the CCAC, (R. 32), and are accepted as true. Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009).

P&G makes tampons and markets some under the brands Tampax Pearl and Tampax Radiant (the “Products”). (R. 32 ¶¶ 1–3.)1 The Products’ labels include certain statements about the Products, including: “#1 GYNECOLOGIST RECOMMENDED TAMPON BRAND,” “FREE OF PERFUME,” “FREE OF ELEMENTAL CHLORINE BLEACHING,” “TAMPON FREE OF DYES,” and “CLINICALLY TESTED GENTLE TO SKIN.” (Id. ¶ 4.) The plaintiffs allege that these statements lead consumers to

1 For ECF filings, the Court cites to the page number(s) in the document’s ECF header unless citing to a particular paragraph or other page designation is more appropriate. believe the Products to be free of potentially harmful ingredients or elements, namely lead. (Id. ¶ 5.) They also allege the statements are misleading and deceptive because they “omit[] and fail[] to disclose that the Products are contaminated with, or at the risk of being contaminated with, substantial levels of lead.” (Id. ¶ 6.) Because, as they allege, consumers are concerned about lead consumption, these statements and omissions regarding the presence of lead are material. (Id. ¶¶ 90–92.)

The plaintiffs further allege that consumption of or exposure to lead in any amount is dangerous. (Id. ¶¶ 38–45.) The dangers are particularly acute when lead is absorbed directly into the bloodstream, which can occur through tampon use. (Id. ¶¶ 46–50.) The plaintiffs’ counsel “conducted independent testing of the Products by established laboratories specializing in chemical analysis of consumer products.” (Id. ¶ 53.) The lab tested “homogenous samples” of the Products, including tampons from boxes purchased personally by some plaintiffs, using an FDA-approved method for testing “the presence of heavy metals in food.” (Id. ¶¶ 51–60.) The results show that “all sizes and varieties” of the Products “uniformly contain a substantial amount of lead,” above the “EPA action level standard for lead in drinking water” and the maximum allowable dose level under California Proposition 65. (Id. ¶¶ 60–67.) As a result, the plaintiffs contend that they paid more for the Products than they would have, had they known the Products contained lead. (Id. ¶¶ 33–39.)

The plaintiffs bring causes of action under the Illinois Consumer Fraud and Deceptive Business Practices Act, 815 ILCS 505/1, et seq. (“ICFA”) (Count I), and a number of similar consumer protection acts from other jurisdictions (Counts II, V–XII). They also bring claims for negligent misrepresentation (Count III), unjust enrichment (Count IV), and breach of implied warranty (Count XIII). The named plaintiffs seek to represent three classes: a nationwide class; a class of citizens of the District of Columbia, Florida, Illinois, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, and New York; and a class of only Illinois citizens. (Id. ¶ 295.)

Analysis

The Court first notes that P&G submitted a notice of supplemental authority, (R. 63), attaching an article published in Toxicological Sciences regarding the health risks of metals in tampons. (R. 63-1.) P&G then filed a “request for judicial notice” of “a printout from the FDA’s website” that summarizes the study. (R. 67; R. 67-1.) A court may take judicial notice of certain matters without converting a motion to dismiss into a motion for summary judgment. Ennenga v. Starns, 677 F.3d 766, 773–74 (7th Cir. 2012). But this only applies to facts “not subject to reasonable dispute.” Mays v. Dart, 974 F.3d 810, 824 (7th Cir. 2020) (citing Fed. R. Evid. 201(b)). While it cannot be reasonably disputed that the study is referenced on the FDA website, the veracity of the study and the conclusions reached therein may be subject to scientific debate and reasonable dispute. See id. (declining to take judicial notice of a CDC report because the content was not “incontrovertible” and was thus reasonably disputable). P&G essentially asks the Court to weigh the evidence it submitted against the plaintiffs’ allegations, which is improper at this stage. Gociman v. Loyola Univ. of Chi., 41 F.4th 873, 885 (7th Cir. 2022) (a Rule 12(b)(6) motion tests the sufficiency, not veracity, of allegations). Accordingly, the Court declines to take judicial notice of the study.

Standing

P&G contests the plaintiffs’ Article III standing to sue. (R. 48 at 10–13.) While P&G does not raise its standing arguments under Rule 12(b)(1), that is how the Court understands them. Bazile v. Fin. Sys of Green Bay, Inc., 983 F.3d 274, 279 (7th Cir. 2020). There are three components to standing: “an injury in fact that is concrete, particularized, and actual or imminent,” “the injury was likely caused by the defendant,” and “the injury would likely be redressed by judicial relief.” TransUnion LLC v. Ramirez, 594 U.S. 413, 423 (2021) (citation omitted). A facial challenge to standing, (see R. 48 at 10–13,) “tests whether the allegations, taken as true, support an inference that the elements of standing exist.” Bazile, 983 F.3d at 279.

P&G argues the injury-in-fact element is lacking because the plaintiffs fail to allege that the Products “actually contain lead at levels that pose a potential health risk.” (Id.) The plaintiffs allege that the Products uniformly contain “substantial” amounts of lead, the labels mislead consumers regarding the presence of lead, and that lead exposure in any amount poses a litany of health and safety risks. (R. 32 ¶¶ 38–67.) As a result, the plaintiffs claim that they paid more for the Products than they would have, had they known of the lead. (Id. ¶¶ 20–21.) This alleged financial harm confers standing. See In re Aqua Dots Prod. Liab. Litig., 654 F.3d 748, 751 (7th Cir. 2011). These allegations differ from those in the cases cited by P&G, which involved alleged defects that varied based on manufacturing site, time, or some other variable. (See R. 48 at 10–11.) Here, the plaintiffs allege a widespread defect impacting every Product. (R.

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Stephanie Foster, Sophie Capshaw-Mack, and Olga Otkina, et al. v. The Proctor & Gamble Company, (N.D. Ill. 2026).

Stephanie Foster, Sophie Capshaw-Mack, and Olga Otkina, et al. v. The Proctor & Gamble Company (Stephanie Foster, Sophie Capshaw-Mack, and Olga Otkina, et al. v. The Proctor & Gamble Company) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

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