F.G. v. CooperSurgical, Inc.

District Court, N.D. California·Decided December 4, 2024·No. 4:24-cv-01261·Unknown

Opinion

1 2 3 4 UNITED STATES DISTRICT COURT 5 NORTHERN DISTRICT OF CALIFORNIA 6 7 F.G., et al., Case No. 24-cv-01261-JST

8 Plaintiffs, ORDER DENYING MOTIONS TO 9 v. DISMISS AND STRIKE

10 COOPERSURGICAL, INC., et al., Re: ECF No. 68, 69 Defendants. 11

12 13 Before the Court is CooperSurgical Inc.’s (“CooperSurgical”) motion to dismiss and 14 CooperSurgical and The Cooper Companies, Inc.’s (“CooperCompanies”) (together, 15 “Defendants”) motion to strike. ECF Nos. 68, 69. The Court will deny the motion to strike and 16 the motion to dismiss as directed to Plaintiffs T.U and V.W. 17 I. BACKGROUND1 18 A. Defendants CooperSurgical and CooperCompanies 19 CooperSurgical and CooperCompanies “manufacture, market, and sell products to fertility 20 clinics, including a culture media product designed to support the growth and development of 21 embryos created through” in vitro fertilization (“IVF”). FAC ¶ 2.2 Embryo culture media is “a 22 nutrient-rich liquid that surrounds a fertilized egg during the incubation period to help it develop 23 into a viable embryo as part of the IVF process.” Id. “Embryo culture media is typically 24 comprised of multiple ingredients including carbohydrates, amino acids, vitamins, magnesium, 25 and growth factors.” Id. ¶ 49. “Magnesium is required for embryonic development and is a key 26 1 For the purpose of resolving CooperSurgical’s motion to dismiss, the Court accepts as true the 27 allegations in the first amended complaint, ECF No. 53 (“FAC”). Knievel v. ESPN, 393 F.3d 1 element to repair mutations during cell division. Insufficient magnesium levels in embryo culture 2 media can cause embryo growth to arrest and inhibit DNA repair.” Id. ¶ 50. 3 On December 5, 2023, CooperSurgical issued a recall notice for three lots of media sold 4 under its Global Media line. Id. ¶¶ 48, 54. The recall notice stated, in part, that “‘CooperSurgical 5 [had] become aware of a sudden increase in complaints regarding the aforementioned lots of this 6 product,’ acknowledged that the ‘risk to health is impaired embryo development prior to the 7 blastocyst stage,’ and directed clinics who purchased the product to quarantine and return it.” 8 Id. ¶ 55. Plaintiffs’ complaint alleges that “Defendants knew or should have known that 9 magnesium is a critical component and essential element of embryo culture media, and that a lack 10 of magnesium in the Global Media may result in the destruction or arrested development of human 11 embryos.” Id. ¶ 57. Plaintiffs contend that “Defendants failed to adequately monitor their 12 manufacturing systems and processes, and allowed for the production of embryo culture media 13 without ensuring that sufficient amounts of magnesium was included.” Id. ¶ 58. Plaintiffs further 14 allege that “Defendants did not properly test or inspect the impacted lots of Global Media until 15 after receiving numerous complaints from fertility clinics that embryos cultured in Defendant’s 16 Global Media were dying at elevated rates.” Id. ¶ 59. 17 B. Plaintiffs F.G. and H.I. 18 Plaintiffs F.G. and H.I. are “a married couple that sought fertility treatment at a fertility 19 clinic in New York, undergoing the invasive, expensive, and emotionally taxing process of IVF in 20 the hopes of having biological children.” Id. ¶ 4. In November 2023, F.G. and H.I.’s fertility 21 clinic “fertilized four of F.G.’s eggs with H.I.’s sperm and placed them in Defendants’ culture 22 media.” Id. ¶ 64. “Each of the four eggs was successfully fertilized, but all of F.G. and H.I.’s 23 developing embryos were destroyed due to Defendants’ defective culture media.” Id. ¶ 65. 24 In February 2024, F.G. and H.I.’s fertility clinic notified them that their embryos were 25 exposed to the culture media subject to a recall and that “[w]hile [CooperSurgical] has not 26 completed the investigation, [CooperSurgical does] believe that the issues observed in the field are 27 likely due to a reduced level of magnesium in the media.” Id. ¶ 66. F.G. is “older now [than] she 1 able to create additional embryos . . . those embryos made with older eggs would not have as high 2 of a chance of successfully developing into a healthy child or children.” Id. ¶ 67. 3 C. Plaintiffs T.U. and V.W. 4 Plaintiffs T.U. and V.W. are a couple who underwent “the expensive and emotionally 5 taxing process of IVF in the hopes of having children. To maximize their chances, [they] secured 6 donor eggs from a young, healthy donors. Their plan was to implant the healthy embryos in 7 Plaintiff T.U.’s uterus so that she could experience carrying their child to term.” Id. ¶ 5. They 8 “engaged in IVF treatment at Zouves Fertility Center in Foster City, California. The IVF process 9 produced six fertilized eggs that were to be developed into viable embryos.” Id. ¶ 69. On 10 December 8, 2023, their fertility clinic “fertilized six of the donor eggs and placed them in 11 Defendants’ culture media.” Id. ¶ 70. 12 “Each of the six eggs was successfully fertilized, but all but one of T.U. and V.W.’s 13 developing embryos were destroyed due to Defendants’ defective culture media. The remaining 14 embryo developed to blastocyst, but was later determined through genetic testing to be 15 chromosomally abnormal and thus unusable.” Id. ¶ 71. 16 In February 2024, T.U. and V.W. were notified by their fertility clinic that their embryos 17 were “exposed to the defective culture media, which was subject to a recall” and that the “quality 18 control issue could have resulted in fewer embryos than [they] would otherwise have made 19 embryo development [sic].” Id. ¶ 72. 20 Plaintiffs allege that the embryos they lost “are irreplaceable” and that T.U. and V.W. “are 21 both older now.” Id. ¶ 73. “As a result, even if Plaintiffs are able to afford to create additional 22 embryos—an emotionally taxing and financially costly procedure that is by no means guaranteed 23 to succeed—those embryos made with older sperm may not have as high of a chance of 24 successfully developing into a healthy child or children, and Plaintiff T.U. faces heightened risks 25 of possible health complications from carrying a child to term.” Id. 26 D. Procedural History 27 Plaintiffs brought this action against Defendants alleging strict products liability 1 gross negligence, trespass to chattels, and unjust enrichment. Id. at 17–24. Plaintiffs brought 2 these claims on behalf of themselves and on behalf of a class composed of “[a]ll individuals in the 3 United States whose eggs and/or embryos were exposed to Recalled Lots of Defendants’ Global 4 Media product (Global Media Lots number 231020-018741, 231020-018742, and 231020- 5 018743).” Id. ¶ 74. Including the present case, there are now at least 39 cases pending before the 6 undersigned making similar claims against Defendants. 7 CooperSurgical and CooperCompanies have each filed separate motions to dismiss but one 8 joint motion to strike the class allegations. ECF Nos. 67, 68, 69. After Defendants filed their 9 motions, the Court issued an Order Granting Defendants’ Motions to Dismiss and Granting 10 Plaintiffs Jurisdictional Discovery in the related case, Walden v. CooperSurgical, 4:24-cv-00903- 11 JST (N.D. Cal. Sept. 9, 2024). In light of the Court’s Walden order, the Court defers ruling on 12 CooperCompanies’ motion to dismiss as well as the portion of CooperSurgical’s motion directed 13 to the non-California Plaintiffs pending the completion of jurisdictional discovery. See ECF No. 14 88 at 2. But the Court will now decide Defendants’ motion to strike and the portion of 15 CooperSurgical’s motion to dismiss directed to T.U. and V.W. See id.; ECF No. 93. 16 II. JURISDICTION 17 Plaintiffs allege this Court has jurisdiction under 28 U.S.C. § 1332(d). 18 III. MOTION TO DISMISS 19 A.

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