Rachel Maher, et al. v. AMAG Pharmaceuticals, Inc.

CourtDistrict Court, D. New Jersey
DecidedJanuary 27, 2026
Docket2:20-cv-00152
StatusUnknown

This text of Rachel Maher, et al. v. AMAG Pharmaceuticals, Inc. (Rachel Maher, et al. v. AMAG Pharmaceuticals, Inc.) is published on Counsel Stack Legal Research, covering District Court, D. New Jersey primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Rachel Maher, et al. v. AMAG Pharmaceuticals, Inc., (D.N.J. 2026).

Opinion

UNITED STATES DISTRICT COURT DISTRICT OF NEW JERSEY

RACHEL MAHER, et al., individually and

on behalf of other similarly situated Civil Action No. 20-152 (JXN)(JBC)

Plaintiffs,

OPINION v.

AMAG PHARMACEUTICALS, INC.,

Defendant.

NEALS, District Judge Before the Court is Plaintiffs’1 unopposed motions for final settlement approval (ECF No. 139), final settlement class approval (id.), and attorneys’ fees, expenses, and service awards (ECF No. 137). The Court carefully considered the parties’ submissions and held an in-person final approval hearing on January 12, 2026 (see ECF No. 142). For the reasons set forth below, the motions are GRANTED. I. BACKGROUND Defendant AMAG Pharmaceuticals (“AMAG”) marketed and sold a drug designed to prevent preterm births (“Drug”). (See Final Approval Joint Decl. ¶ 14, ECF No. 139-3.) The Food and Drug Administration (“FDA”) approved the Drug in 2011. (Id.) After a 2019 study showed the Drug did not work, the FDA withdrew approval in 2023. (Id.)

1 The named Plaintiffs are Rachel Maher, Marina Gomez, Rebecca Torres, Brittany Bonds, Teresa Faughnan, Ebony Odommorris, Molly O’Hara, and Brandy Silas. Plaintiffs in five states sued AMAG, alleging AMAG knew the Drug was ineffective despite marketing it as effective.2 (Id. ¶ 15.) One of those lawsuits was filed in this Court. (Id.) The other four were transferred here and consolidated. (Id.) After this Court partially granted AMAG’s motion to dismiss in 2023, (see Dismissal Op., ECF No. 109), the parties entered

mediation, (Final Approval Joint Decl. ¶¶ 25–26). Mediation succeeded, and the parties signed a Settlement Agreement on May 1, 2025. (Id. ¶ 29; see also Final Approval Mot. Ex. 1 (“Settlement Agreement”), ECF No. 139-3 at *21–46.) The Settlement establishes a $7.5 million fund, representing 48% of the potential damages Settlement Class Members could recover, to be distributed pro rata to claimants. (Final Approval Joint Decl. ¶ 34.) The Settlement Class has 65,000 members. (See id. ¶ 30.) The Court preliminarily approved the Settlement and preliminarily certified the Settlement Class on July 10, 2025. (Preliminary Settlement Approval Op., ECF No. 134.) Thereafter, the parties notified the

Settlement Class. (Final Approval Joint Decl. ¶¶ 47–52.) Thirty class members requested exclusion, and none objected. (Id. ¶¶ 58–60.) The parties now request final approval and class certification. (See Final Approval Moving Br., ECF No. 139-1.) They also request $2,500,000 in attorneys’ fees (representing 33% of the Settlement Fund), $101,625.09 in litigation expenses, and a $5,000 service fee for each named plaintiff. (Fees Award Moving Br., ECF No. 137.) The Court held an in-person final approval hearing on January 12, 2026.

2 AMAG denies these allegations. II. DISCUSSION A. Final Settlement Approval i. Notice Before granting final settlement approval, “[t]he [C]ourt must direct notice in a reasonable

manner to all class members who would be bound by the proposal.” Fed. R. Civ. P. 23(e)(1). The notice must clearly and plainly state (1) “the nature of the action”; (2) “the definition of the class certified”; (3) “the class claims, issues, or defenses”; (4) “that a class member may enter an appearance through an attorney if the member so desires”; (5) “that the court will exclude from the class any member who requests exclusion”; (6) “the time and manner for requesting exclusion”; and (7) “the binding effect of a class judgment on members.” Fed. R. Civ. P. 23(c)(2)(B). Notice must also “satisfy the requirements of due process.” In re Baby Prods. Antitrust Litig., 708 F.3d 163, 180 (3d Cir. 2013).

Here, a third-party administrator sent mail and email notice to the class members. (See Lynch Decl. ¶¶ 6–11, ECF No. 139-2.) The notice clearly and plainly states the information Rule 23(c)(2) requires, such that a class member could make an informed decision about the settlement. (See Notice of Settlement, ECF No. 139-2 at *11–12.) The Court, therefore, is satisfied the class received adequate notice.

ii. Fairness Under Federal Rule of Civil Procedure3 23(e)(2), the Court may grant final approval of a settlement only after a hearing and finding the settlement is “fair, reasonable, and adequate.” Settlement is fair, reasonable, and adequate based on:

3 “Rule” or “Rules” hereinafter refer to the Federal Rules of Civil Procedure. (1) The complexity, expense, and likely duration of the litigation; (2) the reaction of the class to the settlement; (3) the stage of the proceedings and the amount of discovery completed; (4) the risks of establishing liability; (5) the risks of establishing damages; (6) the risks of maintaining the class action through the trial; (7) the ability of the defendants to withstand a greater judgment; (8) the range of reasonableness of the settlement fund in light of the best possible recovery; and (9) the range of reasonableness of the settlement fund to a possible recovery in light of all the attendant risks of litigation. In re Warfarin Sodium Antitrust Litig., 391 F.3d 516, 534–35 (3d Cir. 2004) (quoting Girsh v. Jepson, 521 F.2d 153, 157 (3d Cir. 1975)). Other relevant factors include: the maturity of the underlying substantive issues, as measured by experience in adjudicating individual actions, the development of scientific knowledge, the extent of discovery on the merits, and other factors that bear on the ability to assess the probable outcome of a trial on the merits of liability and individual damages; the existence and probable outcome of claims by other classes and subclasses; the comparison between the results achieved by the settlement for individual class or subclass members and the results achieved—or likely to be achieved—for other claimants; whether class or subclass members are accorded the right to opt out of the settlement; whether any provisions for attorneys’ fees are reasonable; and whether the procedure for processing individual claims under the settlement is fair and reasonable In re Prudential Ins. Co. Am. Sales Prac. Litig. Agent Actions, 148 F.3d 283, 323 (3d Cir. 1998). The Court must also consider whether the settlement provides a “direct benefit to the class.” Baby Prods., 708 F.3d at 178. In this case, all the above factors support final approval. a. Complexity This factor assesses the time and money the parties would spend if litigation continued. In re Gen. Motors Corp. Pick-Up Truck Fuel Tank Prods. Liab. Litig., 55 F.3d 768, 812 (3d Cir. 1995). “By measuring the costs of continuing on the adversarial path, a court can gauge the benefit of settling the claim amicably.” Id. This settlement follows a sprawling, six-year-long, multi-state, pharmaceutical class action lawsuit with 65,000 class members. To maintain the action, the parties would have to conduct voluminous discovery and litigate motions for class certification, summary judgment, and to exclude evidence at trial. The parties would have contested the action at every step. In short, after six years, this case just proceeded past the motion-to-dismiss stage. Bringing it to trial would take many more. This factor, accordingly, favors settlement. b.

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