FEDERAL TRADE COMMISSION v. HEALTH RESEARCH LABORATORIES LLC

CourtDistrict Court, D. Maine
DecidedJuly 31, 2020
Docket2:17-cv-00467
StatusUnknown

This text of FEDERAL TRADE COMMISSION v. HEALTH RESEARCH LABORATORIES LLC (FEDERAL TRADE COMMISSION v. HEALTH RESEARCH LABORATORIES LLC) is published on Counsel Stack Legal Research, covering District Court, D. Maine primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
FEDERAL TRADE COMMISSION v. HEALTH RESEARCH LABORATORIES LLC, (D. Me. 2020).

Opinion

UNITED STATES DISTRICT COURT DISTRICT OF MAINE

FEDERAL TRADE ) COMMISSION, et al., ) ) Plaintiffs, ) ) v. ) 2:17-cv-00467-JDL ) HEALTH RESEARCH ) LABORATORIES, LLC, et al., ) ) Defendants. )

ORDER

The Federal Trade Commission and the State of Maine (collectively, “Plaintiffs”) bring this civil contempt proceeding against Health Research Laboratories, LLC, Kramer Duhon, and Whole Body Supplements, LLC (collectively, “Contempt Defendants”), for alleged violations of Section II.H of the Stipulated Final Judgment and Order previously entered in this action (“the Judgment”). In addition to moving for an Order to Show Cause (ECF No. 21), the Plaintiffs move to modify the Judgment (ECF No. 22). Health Research Laboratories and Duhon cross-move to modify the Judgment (ECF No. 30), and the Contempt Defendants move to stay the contempt proceedings until the cross-motions to modify the Judgment are resolved (ECF No. 31). Pursuant to my orders dated April 1 and April 8, 2020, I now address the threshold question of whether Section II.H of the Judgment is ambiguous on its face as a matter of law. For the reasons explained below, I conclude that Section II.H is facially ambiguous. I. BACKGROUND In a complaint dated November 30, 2017, the Plaintiffs alleged that Duhon and his company, Health Research Laboratories, made deceptive health- and disease-

related claims about several products, including the dietary supplements BioTherapex and NeuroPlus. On January 16, 2018, with the consent of the parties, I approved and entered the Judgment. The Court retained jurisdiction for purposes of construing, modifying, and enforcing the Judgment. The Judgment resolved all matters in dispute in the underlying action, including the complaint’s allegations that Duhon and Health Research Laboratories

violated state and federal law “in connection with the labeling, advertising, marketing, distribution, and sale of products purported to cause weight loss, treat arthritis, relieve joint and back pain, and prevent or mitigate cognitive decline.” ECF No. 15 at 2. The Judgment prohibits Health Research Laboratories, Duhon, and “officers, agents, employees, and all other persons in active concert or participation with any of them, who receive actual notice” of the Judgment, from making several categories of representations. E.g., id. at 6. For example, Section I, entitled “Banned

Weight-Loss Claims,” prohibits seven specific representations about certain products’ ability to cause weight loss in consumers. Id. Section II is entitled “Prohibited Representations: Other Weight-Loss Claims, Joint-Related Disease Claims, and Alzheimer’s Disease, Memory, and Cognitive Performance Claims.” Id. at 7. Section II concerns representations not already prohibited by Section I which state that any Covered Product: (A) causes weight loss;

(B) causes fat loss; (C) treats or cures rheumatism, arthritis, or osteoarthritis; (D) relieves joint pain, back pain, or muscle pain; (E) protects the brain against Alzheimer’s disease or dementia; (F) reverses memory loss; (G) improves memory, concentration, or cognitive performance; or (H) “[c]ures, mitigates, or treats any

disease.” Id. at 8. The Judgment defines “Covered Products” as “any Dietary Supplement, Food, or Drug, including BioTherapex and NeuroPlus.” Id. at 4. In addition to providing definitions of “Dietary Supplement,” “Food,” and “Drug,” the Judgment specifies that “including” means “including but not limited to.” Id. at 4−5. Representations covered by Section II are prohibited unless they are “non- misleading” and substantiated by human clinical testing that is “randomized, double-

blind, . . . placebo-controlled,” and conducted by qualified researchers. Id. at 8−9. Section III, entitled “Prohibited Representations: Other Health-Related Claims,” covers representations “about the health benefits, safety, performance, or efficacy of any Covered Product” beyond those representations already prohibited by Sections I and II of the Judgment. Id. at 9. Representations covered by Section III are prohibited unless they are “non-misleading” and are substantiated by competent and reliable scientific evidence, which is defined as:

[T]ests, analyses, research, or studies (1) that have been conducted and evaluated in an objective manner by experts in the relevant disease, condition, or function to which the representation relates; (2) that are generally accepted by such experts to yield accurate and reliable results; and (3) that are randomized, double-blind, and placebo-controlled human clinical testing of the Covered Product, or of an Essentially Equivalent Product, when such experts would generally require such human clinical testing to substantiate that the representation is true. Id. at 9−10. Additionally, Section IV prohibits certain misrepresentations about scientific certain misrepresentations about endorsements of Covered Products. Finally, Section VIII prohibits seven specific misrepresentations made “in connection with the advertising, marketing, promotion, offering for sale, sale, or distribution of any good

or service.” Id. at 14. The Plaintiffs contend that the Contempt Defendants violated Section II.H of the Judgment by making unsubstantiated claims that four products—Neupathic, Black Garlic Botanicals, BG18, and The Ultimate Heart Formula—cure, treat, or mitigate the following diseases: diabetes, diabetic neuropathy, cardiovascular disease, atherosclerosis, and hypertension. The Contempt Defendants respond that

Section II.H was not intended to cover representations relating to diabetes, diabetic neuropathy, cardiovascular disease, atherosclerosis, and hypertension. In keeping with my procedural order dated April 8, 2020, I now address whether the scope of Section II.H is facially ambiguous. II. LEGAL STANDARD When determining the scope of a consent decree such as the Judgment, courts apply “[o]rdinary contract principles.” Navarro-Ayala v. Hernández-Colón, 951 F.2d

1325, 1339 (1st Cir. 1991). Disputed terms are read “in the context of the decree as a whole.” Quinn v. City of Boston, 325 F.3d 18, 30 (1st Cir. 2003) (citing Newport Plaza Assocs. v. Durfee Attleboro Bank, 985 F.2d 640, 646 (1st Cir. 1993)). Courts consider the language contained within the “four corners” of the decree along with the circumstances surrounding its formation, any technical meaning the words used may have had to the parties, and any other documents expressly incorporated in the

decree. United States v. Charter Int’l Oil Co., 83 F.3d 510, 516−17 (1st Cir. 1996) (citing United States v. Armour & Co., 402 U.S. 673, 681−82 (1971) and United States v. ITT Cont’l Baking Co., 420 U.S. 223, 238 (1975)). If the text of a decree is ambiguous, extrinsic evidence of the parties’ intent may be considered to resolve the

ambiguity. See id. at 519 (citing Brennan v. Carvel Corp., 929 F.2d 801, 808 (1st Cir. 1991)); Navarro-Ayala, 951 F.2d at 1343 n.21. A consent decree is ambiguous if it is “susceptible to reasonable alternative interpretations.” Converse Inc. v. Reebok Int’l Ltd., 328 F. Supp. 2d 166, 176 (D. Mass. 2004) (citing Sportfolio Publ’ns, Inc. v. AT & T Corp., 320 F.3d 75, 79 (1st Cir. 2003)).

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Frulla v. CRA Holdings, Inc.
543 F.3d 1247 (Eleventh Circuit, 2008)
McComb v. Jacksonville Paper Co.
336 U.S. 187 (Supreme Court, 1949)
United States v. Armour & Co.
402 U.S. 673 (Supreme Court, 1971)
Sportfolio Publications, Inc. v. AT & T Corp.
320 F.3d 75 (First Circuit, 2003)
Quinn v. City of Boston
325 F.3d 18 (First Circuit, 2003)
United States v. Saccoccia
433 F.3d 19 (First Circuit, 2005)
Roberto Navarro-Ayala v. Rafael Hernandez-Colon
951 F.2d 1325 (First Circuit, 1991)
Hawkins v. Department of Health & Human Services
665 F.3d 25 (First Circuit, 2012)
In Re Estate of Barrows
2006 ME 143 (Supreme Judicial Court of Maine, 2006)
United States v. ITT Continental Baking Co.
420 U.S. 223 (Supreme Court, 1975)
American Protection Insurance v. Acadia Insurance Co.
2003 ME 6 (Supreme Judicial Court of Maine, 2003)
Converse Inc. v. Reebok International Ltd.
328 F. Supp. 2d 166 (D. Massachusetts, 2004)
OFFICEMAX INC. v. Sousa
773 F. Supp. 2d 190 (D. Maine, 2011)
Ardente v. Standard Fire Insurance Co.
744 F.3d 815 (First Circuit, 2014)
Donald J. Williams v. Linda Williams
2017 ME 94 (Supreme Judicial Court of Maine, 2017)
Scott v. Fall Line Condo. Ass'n
206 A.3d 307 (Supreme Judicial Court of Maine, 2019)
Collins v. Thompson
8 F.3d 657 (Ninth Circuit, 1993)

Cite This Page — Counsel Stack

Bluebook (online)
FEDERAL TRADE COMMISSION v. HEALTH RESEARCH LABORATORIES LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/federal-trade-commission-v-health-research-laboratories-llc-med-2020.