Clean Label Project Foundation v. Garden of Life, LLC

CourtDistrict Court, District of Columbia
DecidedSeptember 23, 2021
DocketCivil Action No. 2020-3229
StatusPublished

This text of Clean Label Project Foundation v. Garden of Life, LLC (Clean Label Project Foundation v. Garden of Life, LLC) is published on Counsel Stack Legal Research, covering District Court, District of Columbia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Clean Label Project Foundation v. Garden of Life, LLC, (D.D.C. 2021).

Opinion

UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA

CLEAN LABEL PROJECT : FOUNDATION, : : Plaintiff, : Civil Action No.: 20-3229 (RC) : v. : Re Document No.: 7 : GARDEN OF LIFE, LLC, : : Defendant. :

MEMORANDUM OPINION

GRANTING DEFENDANT GARDEN OF LIFE, LLC’S MOTION TO DISMISS

I. INTRODUCTION

Plaintiff Clean Label Project Foundation (“CLP”), a non-profit organization, has brought

this action against Garden of Life, LLC (“Garden of Life”), a provider of branded supplements,

alleging that Garden of Life engaged in unlawful trade practices in violation of the District of

Columbia Consumer Protection Procedures Act (“CPPA”). Defendant Garden of Life has

moved to dismiss this suit pursuant to Federal Rule of Civil Procedure 12(b)(1) for lack of

subject matter jurisdiction, and pursuant to Federal Rule of Civil Procedure 12(b)(6) for failure

to state a claim. It argues that CLP lacks Article III standing, that this action infringes on Garden

of Life’s freedom of speech, and that the suit also runs afoul of the primary jurisdiction doctrine,

which would entrust questions of this nature to federal and state regulators. For the reasons

discussed below, the Court concludes that because CLP has not alleged an injury in fact it lacks

standing and, thus, the complaint must be dismissed. II. FACTUAL BACKGROUND

Defendant Garden of Life is a dietary supplement company that sells prenatal vitamins,

including the following product lines: Garden of Life Vitamin Code Raw Prenatal (180ct),

Garden of Life MyKind Organics Prenatal Multi-Certified Organic Whole Food (90ct), Garden

of Life Dr. Formulated Probiotics-Once Daily Prenatal (30ct), Garden of Life Oceans Mom

Prenatal DHA (30ct), Garden of Life MyKind Organics Prenatal Once Daily (30ct), Garden of

Life MyKind Organics Prenatal Once Daily (90ct), and Garden of Life MyKind Organics

Prenatal (30ct) (collectively, “the Products”). See Compl. ¶ 24, ECF No. 1-1. These products

are sold to District of Columbia consumers through retail stores and online marketplaces. Id.

¶¶ 22, 44. CLP alleges that in order to capture the market for prenatal vitamins and supplements,

Garden of Life marketed the Products with descriptions such as “Clean Nourishment for You &

Your Baby Before, During & After Pregnancy,” id. ¶ 21, “Clean is healthy,” id. ¶ 88, and

promises customers that it is “uncompromising about your health,” id. ¶ 90.

CLP is a non-profit public interest organization that describes its mission as “educat[ing]

the public and enabl[ing] consumers to make informed shopping choices,” id. ¶ 37, part of

which includes “bring[ing] truth and transparency to food and consumer products labeling,” id.

¶ 138. To further this mission, in the fall of 2018 CLP caused the purchase of the Products and

had an accredited third-party chemistry laboratory perform quantitative testing. Id. ¶¶ 25, 100–

102. The results found that the Products “contained quantifiable levels of heavy metals as well

as detectable amounts of WHO Class II Pesticides and BPA,” substances that CLP asserts “are

extremely dangerous to a fetus.” Id. ¶ 25–26. CLP contends that in light of these findings,

Garden of Life mislabeled, falsely advertised, and adulterated the products, causing ongoing

harm to D.C. consumers. Id. 112–120.

2 CLP has now brought suit pursuant to the CPPA, D.C. Code § 28-3901 et seq. The

CPPA permits nonprofit organizations to bring actions “on behalf of itself or any of its members,

or on any such behalf and on behalf of the general public,” and also allows “public interest

organization[s]” to bring actions “on behalf of the interests of a consumer or a class of

consumers.” D.C. Code § 28-3905(k)(1)(C), (D). CLP alleges that Garden of Life engaged in

unlawful trade practices under the CPPA when it marketed and sold prenatal vitamin products in

a manner that misled consumers into believing that the products were free of contaminants and

superior to competing products, when in fact they were contaminated with toxic heavy metals,

pesticides, and BPA. Compl. ¶¶ 123–31 (describing violation of D.C. Code § 28-3904). CLP

also alleges that the presence of these contaminants, which are “injurious to health,” render

Garden of Life’s prenatal vitamins “adulterated” in violation of D.C. Code § 48-103. Id. ¶ 132.

CLP asks the Court for the following relief: (1) a declaration that Garden of Life’s

conduct is in violation of the CPPA; (2) an order enjoining this conduct; (3) an order requiring

Garden of Life “to provide corrective advertising to the residents of the District of Columbia that

restores consumers”; (4) an order granting CLP’s “costs and disbursements, including reasonable

attorneys’ fees and expert fees, and prejudgment interest at the maximum rate allowable by law”;

and (5) punitive damages and any further relief deemed just and proper by the Court. Compl. at

28.

III. PROCEDURAL HISTORY

CLP filed this action in the Superior Court for the District of Columbia on August 25,

2020. The case was removed to this Court on November 9, 2020. Notice of Removal, ECF No.

1. That same month, Garden of Life filed a motion to dismiss the complaint. See Def.’s Mot. to

Dismiss (“Def.’s Mot.”), ECF No. 7. The motion is opposed by CLP. See Pl.’s Resp. in Opp’n

3 to Def.’s Mot. to Dismiss (“Pl.’s Opp’n”), ECF No. 10. Garden of Life has also filed a reply.

See Def.’s Reply in Supp. of Def.’s Mot. to Dismiss (“Def.’s Reply”), ECF No. 11. The motion

is now ripe for consideration. 1

IV. LEGAL STANDARD 2

Federal courts are courts of limited jurisdiction and the law presumes that “a cause lies

outside this limited jurisdiction.” Kokkonen v. Guardian Life Ins. Co. of Am., 511 U.S. 375, 377

(1994); see also Gen. Motors Corp. v. EPA, 363 F.3d 442, 448 (D.C. Cir. 2004). On a motion to

dismiss for lack of subject matter jurisdiction pursuant to Rule 12(b)(1), the plaintiff bears the

burden of establishing by a preponderance of the evidence that the court has subject matter

jurisdiction. Lujan v. Defenders of Wildlife, 504 U.S. 555, 561 (1992).

A court resolving a Rule 12(b)(1) motion must “accept[ ] the factual allegations in the

complaint as true,” Jerome Stevens Pharm., Inc. v. FDA, 402 F.3d 1249, 1253–54 (D.C. Cir.

2005), and “must construe the complaint in favor of the complaining party,” Warth v. Seldin, 422

U.S. 490, 501 (1975).

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Clean Label Project Foundation v. Garden of Life, LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/clean-label-project-foundation-v-garden-of-life-llc-dcd-2021.