NOT FOR PUBLICATION
UNITED STATES DISTRICT COURT DISTRICT OF NEW JERSEY
PATRICIA ANN BRYANT,
Plaintiff, Civil Action No. 24-00332 (GC) (RLS)
v. OPINION
EZRICARE, LLC, et al.,
Defendants.
CASTNER, District Judge
THIS MATTER comes before the Court upon Defendants EzriCare, LLC’s and EzriRx, LLC’s Motions to Dismiss Plaintiff’s Complaint. (ECF Nos. 33 & 34.) Plaintiff opposed (ECF Nos. 35 & 36), and Moving Defendants replied (ECF Nos. 37 & 38). The Court has carefully considered the parties’ submissions and decides the matter without oral argument pursuant to Federal Rule of Civil Procedure (Rule) 78(b) and Local Civil Rule 78.1(b). For the reasons set forth below, and other good cause shown, EzriRx’s Motion is DENIED, and EzriCare’s Motion is GRANTED in part and DENIED in part. I. BACKGROUND Plaintiff, a Kentucky resident, claims that her eyes became infected with Pseudomonas Aeruginosa bacteria after using EzriCare artificial tears that she purchased from EzriCare on Amazon.com. (ECF No. 1 at 1-4.1)
1 Page numbers for record cites (i.e., “ECF Nos.”) refer to the page numbers stamped by the Court’s e-filing system and not the internal pagination of the parties. Plaintiff sues EzriCare, the New Jersey-based company that sold her the product (id. at 4); EzriRx, another New Jersey-based company, which allegedly participated in the supply chain (id. at 4-5); Global Pharma Healthcare Private Ltd., the India-based corporation that designed, manufactured, and packaged the product (id. at 5); and Amazon, the online platform where Plaintiff purchased the product, (id.).2
In a 14-count Complaint, Plaintiff asserts claims against all Defendants for strict liability for failure to warn (Count One); strict liability for design or manufacturing defect (Count Two); negligence or gross negligence (Count Three); products liability – negligence for failure to warn (Count Four); products liability – negligence for design or manufacturing defect (Count Five); negligent misrepresentation or omission (Count Six); fraud (Count Seven); fraudulent concealment (Count Eight); breach of express warranty (Count Nine); breach of implied warranty (Count Ten); negligent failure to timely recall (Count Eleven); punitive damages (Count Thirteen); violations of the New Jersey Products Liability Act (NJPLA), N.J. Stat. Ann. § 2A:58C-1 (Count Fourteen). (ECF No. 1 at 13-37.) Plaintiff also asserts claims against EzriCare and EzriRx for violations of
New Jersey’s Consumer Fraud Act (NJCFA), N.J. Stat. Ann. § 56:8-2 (Count Twelve). (ECF No. 1 at 32-34.) EzriCare and EzriRx each moved to dismiss. EzriRx argues that Plaintiff lacks standing against EzriRx and fails to state a claim against EzriRx. (ECF No. 33-1 at 8-11; ECF No. 38 at 4- 6.) EzriCare argues that: (1) Plaintiff’s Complaint is insufficient on its face, (2) Plaintiff’s product liability claims are subsumed by the NJPLA, (3) Plaintiff fails to sufficiently plead a claim for
2 The Court has diversity-based subject-matter jurisdiction under 28 U.S.C. § 1332(a)(1). breach of express warranty, and (4) Plaintiff fails to sufficiently plead a claim under the NJPLA. (ECF No. 34 at 13-26; ECF No. 37 at 5-12.)3 II. LEGAL STANDARDS A. Rule 12(b)(1)—Lack of Subject-Matter Jurisdiction Under Rule 12(b)(1), a court must grant a motion to dismiss if it lacks subject matter
jurisdiction to hear a claim. See Fed. R. Civ. P. 12(b)(1). A motion to dismiss for want of standing is properly brought under Rule 12(b)(1), because “standing is a jurisdictional matter.” Ballentine v. United States, 486 F.3d 806, 810 (3d Cir. 2007). On a motion to dismiss for lack of standing, plaintiff “bears the burden of establishing the elements of standing, and each element must be supported in the same way as any other matter on which the plaintiff bears the burden of proof, i.e., with the manner and degree of evidence required at the successive stages of the litigation.” Id. (citations and internal quotation marks omitted); see also Transunion LLC v. Ramirez, 141 S. Ct. 2190, 2207-08 (2021) (confirming that “plaintiffs must demonstrate standing for each claim that they press and for each form of relief they seek . . . with the manner and degree of evidence
required at the successive stages of the litigation”). In evaluating a Rule 12(b)(1) motion to dismiss, courts must first determine whether the motion “presents a ‘facial’ attack or a ‘factual’ attack on the claim at issue, because that distinction determines how the pleading must be reviewed.” Const. Party of Pa. v. Aichele, 757 F.3d 347, 357 (3d Cir. 2014) (quoting In re Schering Plough Corp. Intron/Temodar Consumer Class Action, 678 F.3d 235, 243 (3d Cir. 2012)). “A facial 12(b)(1) challenge, which attacks the complaint on its face without contesting its alleged facts, is like a 12(b)(6) motion in requiring the court to
3 EzriRx joins in EzriCare’s motion to dismiss. (ECF No. 33-1 at 5 n.1.) ‘consider the allegations of the complaint as true.’” Hartig Drug Co. Inc. v. Senju Pharm. Co., 836 F.3d 261, 268 (3d Cir. 2016) (citation omitted). A factual challenge, on the other hand, “attacks allegations underlying the assertion of jurisdiction in the complaint, and it allows the defendant to present competing facts.” Id.; see Davis v. Wells Fargo, 824 F.3d 333, 346 (3d Cir. 2016) (noting that a motion “supported by a
sworn statement of facts . . . must be construed as a factual, rather than a facial attack” (quoting Int’l Ass’n of Machinists & Aerospace Workers v. Nw. Airlines, Inc., 673 F.2d 700, 711 (3d Cir. 1982))). The party invoking the federal court’s jurisdiction has “the burden of proof that jurisdiction does in fact exist.” Petruska v. Gannon Univ., 462 F.3d 294, 302 n.3 (3d Cir. 2006) (quoting Mortensen v. First Fed. Sav. & Loan Ass’n, 549 F.2d 884, 891 (3d Cir. 1977)). The “trial court is free to weigh the evidence and satisfy itself as to the existence of its power to hear the case” and “the plaintiff will have the burden of proof that jurisdiction does in fact exist.” Id. (quoting Mortensen, 549 F.2d at 891). “Therefore, a 12(b)(1) factual challenge strips the plaintiff of the protections and factual deference provided under 12(b)(6) review.” Hartig Drug Co., 836
F.3d at 268. Regardless of the type of challenge, the plaintiff bears the “burden of proving that the court has subject matter jurisdiction.” Cottrell v. Heritages Dairy Stores, Inc., Civ. No. 09-1743, 2010 WL 3908567, at *2 (D.N.J. Sep. 30, 2010) (citing Mortensen, 549 F.2d at 891). B. Rule 12(b)(6)—Failure to State a Claim On a motion to dismiss for failure to state a claim, courts “accept the factual allegations in the complaint as true, draw all reasonable inferences in favor of the plaintiff, and assess whether the complaint and the exhibits attached to it ‘contain enough facts to state a claim to relief that is plausible on its face.’” Wilson v. USI Ins. Serv. LLC, 57 F.4th 131, 140 (3d Cir. 2023) (quoting Watters v. Bd. of Sch. Directors of City of Scranton, 975 F.3d 406, 412 (3d Cir. 2020)). “A claim is facially plausible ‘when the plaintiff pleads factual content that allows the court to draw the reasonable inference that the defendant is liable for the misconduct alleged.’” Clark v. Coupe, 55 F.4th 167, 178 (3d Cir. 2022) (quoting Mammana v. Fed. Bureau of Prisons, 934 F.3d 368, 372 (3d Cir. 2019)). When assessing the factual allegations in a complaint, courts “disregard legal
conclusions and recitals of the elements of a cause of action that are supported only by mere conclusory statements.” Wilson, 57 F.4th at 140 (citing Oakwood Lab’ys LLC v. Thanoo, 999 F.3d 892, 903 (3d Cir. 2021)). The defendant bringing a Rule 12(b)(6) motion bears the burden of “showing that a complaint fails to state a claim.” In re Plavix Mktg., Sales Pracs. & Prod. Liab. Litig. (No. II), 974 F.3d 228, 231 (3d Cir. 2020) (citing Davis, 824 F.3d at 349). III. DISCUSSION A. EzriRx’s Motion EzriRx argues that the Complaint does not allege facts establishing standing against it. (ECF No. 33-1 at 8-9.) Article III standing requires “(1) an injury-in-fact, (2) a sufficient causal
connection between the injury and the conduct complained of, and (3) a likelihood that the injury will be redressed by a favorable decision.” Finkelman v. Nat’l Football League, 810 F.3d 187, 193 (3d Cir. 2016). EzriRx challenges only the causal-connection element. EzriRx argues that Plaintiff has not and cannot plead a causal connection between her injury and EzriRx, because EzriRx operates a business-to-business online marketplace—it does not sell products to consumers. (ECF No. 33-1 at 5-6, 9.) In support, EzriRx submits the affidavit of Ezriel Green, the founder and chief executive officer of EzriRx. (ECF No. 33-2 at 1-2.)4 Green
4 On a factual attack on subject-matter jurisdiction, such as EzriRx’s, “the court may consider evidence ‘outside the pleadings,’ including ‘affidavits, depositions, and testimony to resolve factual issues bearing on jurisdiction.’” Fort v. United States, 712 F. Supp. 3d 575, 587 states that “EzriRx is an online marketplace platform that assists pharmacies in purchasing prescription medications, over-the-counter drugs, and pet medication,” and that “EzriRx does not sell directly to consumers.” (Id. at 1.) Plaintiff asserts that “EzriRx’s Motion suggests—but notably does not state outright—that selling the EzriCare Product to retailers on EzriRx.com is the extent of EzriRx’s involvement with
the EzriCare Product.” (ECF No. 35 at 15.) She also argues that “EzriCare” is a trademark registered and licensed to EzriRx. (Id. at 16.) Plaintiff further asserts that EzriRx and EzriCare share the same leadership, counsel in this litigation, and phone numbers. (Id. at 15.) The Court disagrees with what appears to be an alter-ego theory of liability. Entities sharing leadership, contact information, and counsel, (see id.), does not alone justify disregarding their corporate separateness. See Mikhail v. Amarin Corp., plc, Civ. No. 23-01856, 2024 WL 863427, at *6-8 (D.N.J. Feb. 29, 2024) (discussing the standard for disregarding corporate separateness). The Court cannot disregard EzriRx’s and EzriCare’s separateness on these grounds. On the other hand, the Court finds that the Complaint includes enough allegations from
which the Court could infer a plausible causal connection between Plaintiff’s injury and EzriRx’s conduct. As to EzriRx’s involvement, the Complaint alleges that EzriRx “markets, advertises, labels, distributes, and sells” EzriCare’s artificial tears; and “‘EzriCare’ is a trademark registered and licensed to” EzriRx. (ECF No. 1 at 4-5.) Those allegations explain EzriRx’s connection with EzriCare and the product. They imply the way in which EzriRx may be involved in the design, labeling, advertising, or distribution of a product that made its way to Plaintiff. The Court too observes that Green’s affidavit does not address this issue. (See ECF No. 33-2 at 1-2.) So,
(D.N.J. 2024) (quoting Constitution Party of Pa. v. Aichele, 757 F.3d 347, 358 (3d Cir. 2014); and then Gotha v. United States, 115 F.3d 176, 179 (3d Cir. 1997)). although Plaintiff, faced with a factual challenge on subject-matter jurisdiction, does not enjoy Rule 12(b)(6) deference, the Court finds that her pleadings clear the standing hurdle. In the same light, the Court rejects EzriRx’s Rule 12(b)(6) challenge asserting that the Complaint does not provide “fair notice of the claim and the grounds upon which it rests.” (ECF No. 33-1 at 7, 10.) EzriRx’s Motion to Dismiss is therefore denied.
B. EzriCare’s Motion 1. Group Pleading EzriCare argues that Plaintiff’s Complaint is insufficient on its face because it contains impermissible group pleading. (ECF No. 34 at 14; ECF No. 37 at 5-6.) Specifically, EzriCare argues that the Complaint “fail[s] to give EzriCare notice as to what, if any, claims they make against it because Plaintiff’s Complaint impermissibly lumps all the defendants together.” (ECF No. 34 at 14.) A group pleading “is a complaint that ‘fails to specify which of the defendants are responsible for which acts or omissions, or which of the defendants the claim is brought against.’”
Foulke v. Twp. of Chery Hill, Civ. No. 23-02543, 2024 WL 3568841, at *7 (D.N.J. July 29, 2024) (quoting Morales v. New Jersey, Civ. No. 21-11548, 2023 WL 5003891, at *4 (D.N.J. Aug. 3, 2023)). Group pleadings are those in which “it is ‘virtually impossible to know which allegations of fact are intended to support which claim(s) for relief.’” Innovative Cosm. Concepts, LLC v. Brown Packaging, Inc., Civ. No. 18-5939, 2020 WL 7048577, at *2 (D.N.J. Apr. 28, 2020) (citation omitted). Courts in the Third Circuit often cite to the Eleventh Circuit when addressing group pleading issues. See Foulke, 2024 WL 3568841, at *7 (noting that “it is the Eleventh Circuit that has the robust doctrine prohibiting [group] pleadings”); Bartol v. Barrowclough, 251 F. Supp. 3d 855, 859 n.3 (D.N.J. 2017) (“The United States Court of Appeals for the Eleventh Circuit has articulated the bulk of existing law in [the] area” of group pleadings.). As the Eleventh Circuit recently explained, there are four broad categories of group pleading that merit dismissal: (1) “a complaint containing multiple counts where each count adopts the allegations of all preceding counts,” (2) a complaint that is “replete with conclusory, vague, and immaterial facts not obviously
connected to any particular cause of action,” (3) a complaint that does not separate “into a different count each cause of action or claim for relief,” or (4) a complaint that “assert[s] multiple claims against multiple defendants without specifying which of the defendants are responsible for which acts or omissions, or which of the defendants the claim is brought against.” See Weiland v. Palm Beach Cty. Sheriff’s Office, 792 F.3d 1313, 1321-23 (11th Cir. 2015). The Court is satisfied that Plaintiff’s Complaint is not an impermissible group pleading because each count in the Complaint outlines specific allegations of fact intended to support her claims for relief. See Innovative Cosm. Concepts, LLC, 2020 WL 7048577, at *2. Further, while the Court recognizes that the Complaint contains “multiple counts where each count adopts the
allegations of all preceding counts” and “assert[s] multiple claims against multiple defendants,” Weiland, 792 F. 3d at 1321-23, the Complaint sets forth factual allegations against EzriCare separate from factual allegations against other Defendants throughout the Complaint, such as distinctions in the supply chain of EzriCare artificial tears. (See, e.g., ECF No. 1 at 4-6, 10-12); see also S.S. v. Hillsborough Twp. Bd. of Ed., Civ. No. 20-13077, 2022 WL 807371, at *5 (D.N.J. Mar. 17, 2022) (noting that “courts must consider the complaint in its entirety” (quoting Kedra v. Schroeter, 876 F. 3d 424, 441 (3d Cir. 2017))). Therefore, the Complaint, while not perfect, does not constitute a group pleading and provides EzriCare fair notice of the claims against it. See also Mosley v. EzriCare LLC, 2024 WL 1342615, at *12-13 (E.D. Ky. Mar. 29, 2024) (“The overlapping allegations against the defendants do not transform the [a]mended [c]omplaint into a [group] pleading; the allegations are similar because the premise of the Amended Complaint is that EzriCare and its co-defendants engaged in similar conduct. At this point, before discovery and before more is known about each defendant’s role in getting the relevant products to the market, the Amended Complaint is sufficient.”); Diamond Resorts U.S. Collection Dev., LLC v.
Sumday Vacations, LLC, 2020 WL 3250130, at *2 (M.D. Fla. Feb. 21, 2020) (finding that a complaint alleging the defendants engaged in the same or similar conduct was not an improper group pleading that warranted dismissal). 2. NJPLA Subsumption EzriCare argues that the NJPLA subsumes Plaintiff’s common-law products-liability claims. (ECF No. 34 at 16-18.) Plaintiff counters that it is too early to conduct a choice of law analysis. (ECF No. 36 at 16.) Although “it can be inappropriate or impossible for a court to conduct [a choice of law] analysis at the motion to dismiss stage when little or no discovery has taken place[,] . . . [s]ome
choice of law issues may not require a full factual record and may be amenable to resolution on a motion to dismiss.” Rapid Models & Prototypes, Inc. v. Innovated Sols., 71 F. Supp. 3d 492, 499 (D.N.J. 2014) (quoting Snyder v. Farnam Companies, Inc., 792 F. Supp. 2d 712, 718 (D.N.J. 2011)) (most alterations in Rapid Models). On the present record, the Court finds that it would be inappropriate to conduct a choice- of-law analysis at this stage. To the extent a conflict exists (or does not exist) between the law of New Jersey and Kentucky, the parties do not conduct a choice-of-law analysis for the Court’s review. Nor do they provide the information necessary for the Court to perform its own analysis. See Harper v. LG Elec. U.S.A., Inc., 595 F. Supp. 2d 486, 490 (D.N.J. 2009) (noting that the court was “unable to make the fact-intensive choice-of-law determination on the record before it”); see also Tjahjono v. Westinghouse Air Brake Tech. Corp., 2024 WL 1287085, at *5 (W.D. Pa. Mar. 26, 2024) (noting that “when confronted with a choice of law issue at the motion to dismiss stage, courts within the Third Circuit have concluded that it is more appropriate to address the issue at a later stage in the proceedings”). The Court will refrain from doing so.5 Therefore, the Court rejects
EzriCare’s NJPLA subsumption argument without prejudice subject to EzriCare renewing the argument later. 3. Express Warranty Claim Count Nine asserts a claim for breach of express warranty. To state a claim for breach of express warranty under New Jersey law,6 a plaintiff must allege that (1) “Defendant made an affirmation, promise or description about the product;” (2) “this affirmation, promise or description became part of the basis of the bargain for the product;” and (3) “the product ultimately did not conform to the affirmation, promise or description.” Hindermyer v. B. Braun Med Inc., 419 F. Supp. 3d 809, 829-30 (D.N.J. 2019) (quoting Snyder, 792 F. Supp. 2d at 721). The New
Jersey Uniform Commercial Code (U.C.C.) defines an “express warranty” as follows: (a) Any affirmation of fact or promise made by the seller to the buyer which relates to the goods and becomes part of the basis of the bargain creates an express warranty that the goods shall conform to the affirmation or promise.
5 EzriCare raises the choice of law issue in a footnote. Courts generally need not address arguments raised in footnotes. See Kislak Co. Inc. v. Prominent Properties LLC, Civ. No. 22- 2482, 2023 WL 5218085, at *3 n.1 (D.N.J. Aug. 15, 2023) (“[A]rguments raised in passing (such as, in a footnote), but not squarely argued, are considered waived.” (quoting John Wyeth & Brother Ltd. v. Cigna Int’l Corp., 119 F.3d 1070, 1076, n.6 (3d Cir. 1997))).
6 When sitting in diversity, the Court applies the law of the forum state. See Gebhardt v. Beri, Civ. No. 23-3008, 2024 WL 3279531, at *2 n.2 (D.N.J. June 14, 2024) (citing Erie Railroad v. Tompkins, 304 U.S. 64, 78 (1938)). (b) Any description of the goods which is made part of the basis of the bargain creates an express warranty that the goods shall conform to the description.
[N.J. Stat. Ann. § 12A:2-313(1).]
The Complaint includes a copy of the product’s label. (ECF No. 1 at 7.) On the EzriCare label, it described the product as “Lubricant Eye Drops” that “Refresh, Lubricate and Moisturizes.” (Id. 7-8.) Further, the label lists “Uses” and states the following: “for use as a protectant against further irritation or to relieve dryness of the eye” and “for the temporary relief of discomfort due to minor irritations of the eye, or to exposure to wind or sun.” (Id.) The Complaint asserts that “[s]uch statements constitute an affirmation of fact or promise or a description of the product as being safe and not posing a dangerous health risk.” (Id. at 28.) Additionally, the Complaint argues that “Defendants breached this express warranty because the EzriCare Artificial Tears are not safe.” (Id.) To the contrary, Plaintiff argues that “these artificial tears pose a serious and dangerous health risk because they are contaminated with the Pseudomonas Aeruginosa bacteria—a dangerous and deadly bacterium.” (Id.) Finally, Plaintiff alleges that she “read and relied on these express warranties provided by Defendants in the labeling, packaging, and advertisements.” (Id.) The statements Plaintiff relies on are insufficient to state a claim for breach of express warranty. Courts in this Circuit have refused to find that user instructions, or even labels representing that a product is “safe and effective,” are express warranties. See In re Avandia Mktg. Sales Pracs. & Prod. Liab. Litig., 588 F. App’x 171, 176-78 (3d Cir. 2014) (noting approvingly that an Ohio court “refused to find the words ‘safe and effective’ to create an express warranty in the absence of representations that a drug was free from all harmful side effects or was absolutely harmless”); Volin v. Gen. Elec. Co., 189 F. Supp. 3d 411, 421 (D.N.J. 2016) (rejecting that instructions in an owner’s manual constituted an express warranty that the product would be “free from defects in material and workmanship and fit for the ordinary purpose” of the product). Also relevant is that the EzriCare product label qualifies itself, warning users to “[s]top use and ask a doctor if you experience” “eye pain,” “changes in vision,” or “continued redness or irritation of the eye or if the condition worsens or persists for more than 72 hours.” (ECF No. 1 at 7-8.) See
In re Avandia, 588 F. App’x at 178 (“Because GSK disclosed Avandia’s contraindications, risk factors, and potential side effects and [the plaintiff] does not allege GSK made unqualified guarantees of safety or effectiveness, [the plaintiff] has failed as a matter of New Jersey law to state an express warranty claim.”). Thus, the Court finds that Plaintiff does not state a claim for breach of express warranty under New Jersey law. 4. NJPLA Claim Count Fourteen asserts NJPLA violations for the defective design and manufacturing of EzriCare artificial tears. (ECF No. 1 at 35-37.)
To prove a defect, a plaintiff must show that “(1) the product was defective; (2) the defect existed when the product left the hands of the defendant; (3) the defect proximately caused injuries to the plaintiff; and (4) the injured plaintiff was a reasonably foreseeable user.” Hindermyer, 419 F. Supp. 3d at 823 (citing Myrlak v. Port Auth. of N.Y. & N.J., 723 A.2d 45, 52 (N.J. 1999)). a. Design Defect To establish a prima facie case of design defect, the plaintiff must prove the availability of a “technologically feasible and practical alternative design that would have reduced or prevented the plaintiff’s harm without substantially impairing the reasonably anticipated or intended function of the product.” Hindermyer, 419 F. Supp. 3d at 823-24 (citation omitted). No per se rule requires a plaintiff to, “under all circumstances, provide a reasonable alternative design” at the pleading stage. Id. at 824. But to state a claim for design defect under the NJPLA, the plaintiff must “plead either that the product’s risk [of harm] outweighs its [utility], or that an alternate design exists.” Id. (quoting Mendez v. Shah, 28 F. Supp. 3d 282, 298 (D.N.J. 2014) (alterations in Hindermyer). EzriCare argues that Plaintiff “fails to plead any of the requisite elements for design
defect.” (ECF No. 34 at 22.) The Court disagrees. Plaintiff attributes the contamination to the “lack of appropriate microbial testing, formulation issues[,] . . . and lack of proper controls concerning tamper-evident packaging.” (ECF No. 1 at 2, 11.) For alternative design, Plaintiff asserts that “safer alternatives, including artificial tears products that contain preservatives to prevent the growth of bacteria, have been readily available for decades.” (Id. at 16, 22.) She also alleges that the “‘multi-use’ bottle that is meant to be re-used . . . is preservative free [and] could create a perfect storm for bacterial growth in the bottle/container.” (Id. at 6, 11, 18, 22, 35.) Plaintiff also contends that “new therapies . . . known as ‘phage’ therapies” can be used to “treat antibiotic-resistant bacteria, like the Pseudomonas Aeruginosa[,] . . . by deploying viruses that aim
to attack bacteria, fending off infections that traditional antibiotic drugs fail to stamp out.” (Id. at 9.) And as to the risk-utility element, Plaintiff alleges that “EzriCare Artificial Tears is an inessential over-the-counter product that does not treat or cure any serious disease.” (Id. at 16.) Thinner allegations than these have survived motions to dismiss. See, e.g., Barrett, 518 F. Supp. 3d at 826 (denying a motion to dismiss a defective-design claim alleging that a pharmaceutical “was developed, mixed and/or created in an insanitary and unsafe environment that contained or promoted the development of harmful organisms such as bacteria, which was . . . unreasonably dangerous”). Thus, Plaintiff’s claim for design defect under the NJPLA may proceed. b. Manufacturing Defect A manufacturing defect exists if a product “deviated from the design specification, formulae, or performance standards of the manufacturer or from otherwise identical units manufactured to the same manufacturing specifications or formulae.” N.J. Stat. Ann. § 2A:58C-
2(a). “To determine whether a product contains a manufacturing defect, the ‘product may be measured against the same product as manufactured according to the manufacturer’s standards.’” Hindermyer, 419 F. Supp. 3d at 824 (quoting Mendez, 28 F. Supp. 3d at 298). “If the particular product used by the plaintiff fails to conform to those standards or other units of the same kind, it is a manufacturing defect.” Id. (quoting Mendez, 28 F. Supp. 3d at 298). New Jersey products-liability law does not require the injured plaintiff “to prove a specific manufacturer’s defect.” Id. (quoting Mendez, 28 F. Supp. 3d at 297). “[B]ecause the evidence of a flaw in the manufacturing process is uniquely within the knowledge and control of the manufacturer, ‘[p]roof that a product is not fit for its intended purposes requires only proof . . . that
something was wrong with the product.’” Id. (quoting Myrlak, 723 A.2d at 52) (some quotation marks omitted); see Cole v. NIBCO, Inc., Civ. No. 13-7871, 2016 WL 10536025, at *16 (D.N.J. Feb. 26, 2016) (“[A] plaintiff may demonstrate that a manufacturing defect exists with evidence that in a general sense and as understood by a layman . . . ‘something was wrong’ with the product.” (quoting Scanlon v. Gen. Motors Corp., Chevrolet Motor Div., 326 A.2d 673, 677 (N.J. 1974)). That said, the “mere occurrence of an accident and the mere fact that someone was injured are not sufficient to demonstrate the existence of a defect.” Hindermyer, 419 F. Supp. 3d at 824 (quoting Myrlak, 723 A.2d at 52). Based on these pleading standards and a liberal reading of her Complaint, Plaintiff’s manufacturing-defect allegations are sufficient to survive a motion to dismiss. Plaintiff alleges that the manufacturer failed to perform “appropriate microbial testing” and lacked “proper controls concerning tamper-evidence packaging.” (ECF No. 1 at 2, 11, 18, 35.) She also alleges that the EzriCare product “deviated from the design specifications, formulae, or performance standards of
the manufacturer,” such that the product had been contaminated by the time she used it. (Id. at 37.) As a result, the allegations create a plausible inference that the product “fail[ed] to conform to standards or other units of the same kind.” Cf. Hindermyer, 419 F. Supp. 3d at 824. Thus, Plaintiff’s manufacturing-defect claim under the NJPLA may proceed. 5. NJPLA’s Immunity Provision Although product sellers are subject to liability under the NJPLA, the Act includes an immunity provision “to rescue persons it categorized as ‘product sellers’ from strict liability in certain circumstances.” Allstate New Jersey Ins. Co. v. Amazon.com, Inc., Civ. No. 17-2738, 2018 WL 3546197, at *6 (D.N.J. July 24, 2018) (quoting Thomas v. Ford Motor Co., 70 F. Supp. 2d
521, 530 (D.N.J. 1999)). Thus, “by filing an affidavit correctly identifying the manufacturer of the product,” a defendant seller can escape liability under the Act. Id.; N.J. Stat. Ann. § 2A:58C- 9(b). Even when a product seller submits the affidavit certifying the correct identity of the manufacturer, a product seller may still be liable if the seller “exercised some significant control over the design, manufacture, packaging or labeling of the product relative to the alleged defect in the product which caused the injury, death or damage[; or] . . . if [t]he manufacturer has no known agents, facility, or other presence within the United States[;] or [t]he manufacturer has no attachable assets or has been adjudicated bankrupt and a judgment is not otherwise recoverable from the assets of the bankruptcy estate.” Claypotch v. Heller, Inc., 823 A.2d 844, 852 (N.J. Super. Ct. App. Div. 2003) (quoting N.J. Stat. Ann. § 2A:58C-9(c)(2), (3), (d)(1)). A product seller also may be subject to liability “if it ‘knew or should have known of the defect in the product which caused the injury, death or damage or the plaintiff can affirmatively demonstrate that the product seller was in possession of facts from which a reasonable person would conclude that the product seller had or should have had knowledge of the alleged defect in the product which caused the
injury, death or damage; or . . . created the defect in the product which caused the injury, death or damage.’” Id. (quoting N.J. Stat. Ann. § 2A:58C-9(d)(2), (3)). Therefore, “a product seller is relieved from liability only if it is ‘truly innocent of responsibility for the alleged product and the injured party must retain a viable claim against the manufacturer.’” Bashir v. Home Depot, Civ. No. 08-04745, 2011 WL 3625707, at *3 (D.N.J. Aug. 16, 2011) (quoting Claypotch, 823 A.2d at 852) (emphasis added). EzriCare claims to fall within the NJPLA provision of immunity because it submits an affidavit of Ezriel Green, who is also EzriCare’s co-founder, stating that “EzriCare’s Artificial Tears were manufactured and packaged by Global Pharma Healthcare Private Limited, whose
manufacturing facility is located in Tamil Nadu, India.” (ECF No. 34-2 at 1.) Plaintiff counters and asserts that “EzriCare knew or should have known of the contamination in the Product that caused Plaintiff’s injury because, as the product bore its brand, it had a duty to ensure its product— that was sold and intended for use to relieve discomfort in the human eye—was safe and not contaminated with a dangerous bacterium.” (ECF No. 36 at 26.) The Court finds that the “present record does not establish that EzriCare is ‘truly innocent of responsibility for the alleged product’ as a matter of law,” and therefore the parties should engage in discovery to clarify EzriCare’s role in bringing this product to the market. See Dickstein EzriCare, Civ, No. 23-01649, 2024 WL 2803026, at *10 (D.N.J. May 31, 2024). ‘Thus, the Court rejects EzriCare’s claim of immunity at this time, IV. CONCLUSION For the reasons set forth above, and other good cause shown, EzriRx’s Motion is DENIED, and EzriCare’s Motion is GRANTED in part and DENIED in part. Plaintiffs claim for breach of express warranty is DISMISSED without prejudice. An appropriate Order follows.
Dated: December ff. 2024 ( Leu f f patie GEORGETYE CASTNER UNIT ED STATES DISTRICT JUDGE