CLF 007 v. CooperSurgical, Inc.

CourtDistrict Court, D. Oregon
DecidedMarch 31, 2025
Docket6:24-cv-00990
StatusUnknown

This text of CLF 007 v. CooperSurgical, Inc. (CLF 007 v. CooperSurgical, Inc.) is published on Counsel Stack Legal Research, covering District Court, D. Oregon primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
CLF 007 v. CooperSurgical, Inc., (D. Or. 2025).

Opinion

IN THE UNITED STATES DISTRICT COURT

FOR THE DISTRICT OF OREGON

EUGENE DIVISION

CLF 007, an individual; CLF 008, an individual, Civ. No. 6:24-cv-0990-AA

Plaintiffs, OPINION & ORDER

vs.

COOPERSURGICAL, INC.; THE COOPER COMPANIES, INC.,

Defendants. _______________________________________

AIKEN, District Judge: Plaintiffs CLF 007 and CLF 008, individuals, bring claims in strict products liability, negligence, gross negligence, unjust enrichment, and trespass to chattels against Defendants CooperSurgical, Inc. and The Cooper Companies, Inc. See Compl., ECF No. 1. Defendant CooperSurgical, Inc. moves to dismiss for failure to state a claim under Rule 12(b)(6), ECF No. 24. Defendant Cooper Companies, Inc. moves to dismiss the case for lack of personal jurisdiction under Rule 12(b)(2), ECF No. 19, and for failure to state a claim under Rule 12(b)(6), ECF No. 25. For the reasons explained below, CooperSurgical, Inc.’s Motion to Dismiss, ECF No. 24, is GRANTED in part and DENIED in part. The Court DEFERS ruling on The Cooper Campanies, Inc.’s Motion to Dismiss for lack of personal jurisdiction, ECF No. 19, and its Motion to Dismiss for failure to state a claim, ECF No. 25. Plaintiffs shall have 90 days to conduct limited discovery consistent with this Opinion. BACKGROUND

The Cooper Companies, Inc. (“Cooper Companies”) is the parent company of Cooper Medical Inc., which is the parent company of wholly owned subsidiary CooperSurgical Inc. (“CooperSurgical”). Def. Mot. at 1, 2, 15; Avery Decl. ¶¶ 6–7, Ex. A, ECF No. 19-1. Cooper Companies is incorporated in Delaware and has its principal place of business in California. Def. Mot. at 12. Plaintiffs CLF 007 (“Plaintiff 007”) and CLF 008 (“Plaintiff 008”), a married

couple who reside in Oregon, “have attempted to conceive naturally[],” for fifteen years but without success, so they turned to in vitro fertilization (“IVF”), an assisted reproductive technology (“ART”). Compl. ¶ 45, 1, 2. In November 2023, at age 40, Plaintiff 007 underwent an egg-retrieval procedure that successfully yielded nineteen eggs. Id. at ¶ 46. “From those [nineteen] eggs, fifteen fertilized embryos were created using Plaintiff 007’s eggs and Plaintiff 008’s sperm.” Id. at ¶ 47. “Plaintiffs were incredibly excited that they [might] have a high number of embryos reach [the]

blastocyst [stage] on Day 5 [after fertilization,]” at which time they could be implanted in Plaintiff 007’s uterus. Id. at ¶¶ 47, 21, 24, 25. “Plaintiffs’ excitement was short-lived [because] Plaintiffs doctor informed them that none of their fifteen fertilized embryos had made it to blastocyst on Day 5[,]” an “incredibly devastating and unusual result.” Id. at 48 (emphasis in original). At Day 6 after fertilization, some of Plaintiffs’ remaining embryos, though late in development, had reached the blastocyst stage. Id. at ¶ 49. After genetic testing of those embryos, “Plaintiffs discovered that they had one genetically normal embryo, which they later discovered was a boy.” Id. at ¶ 50. “Although Plaintiffs had hoped

for more viable embryos, they were so excited for their ‘baby boy.’” Id. “At this point, Plaintiffs believed that their low numbers were solely the fault of their own genetic material.” Id. “A month after Plaintiff 007’s [egg] retrieval,” Plaintiffs’ doctor informed Plaintiffs that, after the egg retrieval, their embryos had been placed in an embryo culture media manufactured by Defendants that had been recalled on December 5,

2023, because it was “deficient” in magnesium, a “crucial nutrient” for embryo survival and development Id. at ¶ 51, 59–62. “[G]iven the [‘boy’ embryo’s] exposure [to the recalled embryo culture]” and that “there [was] no good information on whether [that] embryo was usable or if it was likely to have developmental or other defects in pregnancy or later in life[,]” Plaintiffs decided to not transfer that embryo to Plaintiff 007’s uterus. Id. at ¶ 51. Plaintiffs’ failed round of IVF “severely impacted” Plaintiffs’ ability to have

children. Id. at ¶ 52. The fertility procedures took a “physical toll,” especially on Plaintiff 007, who underwent “a variety of hormone[] and medication[]” injections “to stimulate the ovaries and develop eggs[,]” id. at ¶¶ 52, 21, injections that can cause side effects such as injection site complications and, “bloating, weight gain, water retention, bone loss, fatigue, headaches, muscle aches, abdominal pain, breast tenderness, vaginal yeast infections, vaginal dryness, . . . hot flashes, mood swings, depression, nausea, vomiting, diarrhea, clots in blood vessels and strokes[,]” id. at ¶ 22. Plaintiff 007 also underwent “frequent transvaginal ultrasound monitoring and other tests to monitor egg development,” and, finally, an egg retrieval process, “a

surgery to collect the eggs,” done under anesthesia and involving a large needle inserted through the vaginal wall. Id. at ¶ 23. “Plaintiffs [also] expended significant financial resources to undergo these fertility procedures.” Id. at ¶ 52. They “sold one of their cars[,]” “spent months saving up—feeling that this cycle was their “last shot” at being parents[,]” and “used up much of their available time-off balances at work to attend their various

appointments and procedures.” Id. at ¶ 53. Despite Plaintiff 007’s “advanced age,” Plaintiffs decided “to undergo another IVF cycle[,]” causing further “financial strain” and “particular toll on Plaintiff 007, who must again subject herself to the many medications required to prepare for [egg] retrieval.” Id. at ¶ 57. “Plaintiffs want to feel excited and hopeful for the results of their cycle—but they already feel defeated.” Id. “Plaintiff 007’s advanced age” means that they “have a significantly lower chance of yielding any useable embryos.” Id.

Plaintiffs’ “loss ha[s] caused both Plaintiffs . . . emotional distress, . . . deep sadness, guilt, hopelessness, shame, disappointment, and anger.” Id. at ¶ 58. They “struggle to find the confidence to continue with this emotionally taxing journey.” Id. Plaintiffs allege that Defendants CooperSurgical and Cooper Companies “manufactured, marketed, promoted, distributed, and/or sold media to be used for culturing and development of human embryos, [and] marketed that their media provided ‘an optimized in vitro environment,’ which is necessary to ensure that fertilized human eggs can survive and develop into embryos viable for implantation.” Id. at ¶¶ 4, 12, 14, 63, 72. Plaintiffs also allege that Defendants “represented that

they properly and adequately tested their embryo culture media before” selling and distributing the media to “clinics and/or healthcare practitioners[.]” Id. at ¶ 5. Plaintiffs allege that the recalled lots of Defendants’ culture media were deficient in magnesium because the hoppers at Defendants’ manufacturing plants ran out of magnesium but that Defendants produced and sold several lots of that defective media, including the media used by Plaintiffs. Id. at ¶¶ 42, 62, 64, 65.

Plaintiffs allege that “[m]agnesium is a critical ingredient of embryo culture media” because it is “an essential nutrient in embryonic and human fetal growth.” Id. at ¶ 27. Plaintiffs allege that after egg retrieval, eggs are “immersed, typically in a petri dish” that contains the culture media, they are then fertilized and develop in the lab. Id. at ¶ 26. While in the petri dish, the eggs are supported and protected in the early stages of development by the embryo culture media, “just as a woman’s body would do during natural conception.” Id. at ¶ 29.

Plaintiffs allege that the defective culture media “was almost certainly the cause of the damage and destruction of Plaintiffs’ . . . embryos[,]” id. at ¶¶ 51, 85, 86, and that “the new [IVF] cycle [was] necessitated by Defendant’s faulty product[,]” id. at ¶ 58.

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CLF 007 v. CooperSurgical, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/clf-007-v-coopersurgical-inc-ord-2025.