Spurlock v. Wexford Health Sources, Incorporated

District Court, S.D. West Virginia·Decided July 24, 2025·No. 3:23-cv-00476·Unknown

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE SOUTHERN DISTRICT OF WEST VIRGINIA

HUNTINGTON DIVISION

LAUREN SPURLOCK; HEATHER SMITH; and SHAWN ZMUDZINSKI, individually and on behalf of all other similarly situated,

Plaintiffs,

v. CIVIL ACTION NO. 3:23-0476

WEXFORD HEALTH SOURCES, INCORPORATED,

Defendant.

MEMORANDUM OPINION & ORDER Before the Court is Plaintiffs’ Motion for Class Certification, ECF No. 137. Plaintiffs request the Court certify a Damages Class pursuant to Rule 23(b)(3) and an Injunctive Relief Class pursuant to Rule 23(b)(2). For the reasons that follow, the Court GRANTS Plaintiffs’ Motion for Class Certification but modifies the proposed class definitions. BACKGROUND “[T]he opioid epidemic has led to ‘an extraordinary public health crisis that started at least two decades ago and has accelerated over the past decade.’” City of Huntington v. AmerisourceBergen Drug Corp., 96 F.4th 642, 647 (4th Cir. 2024) (citing City of Huntington v. AmerisourceBergen Drug Corp., 609 F. Supp. 3d 408, 419 (S.D.W. Va. 2022) (Faber, J.)). This case centers on a correctional health care company’s response to that acceleration. Wexford Health Sources has contracted with state and local authorities to provide comprehensive health care services in approximately 100 correctional facilities across 11 states. Def.’s Resp. at 3. More than a third of Wexford’s patients suffer from Opioid Use Disorder (OUD), according to the company’s representative. Pls.’ Ex. 8 (Matus Dep.) at 74-76. Plaintiffs allege that Wexford had a uniform policy and practice of denying medication for Opioid Use Disorder (MOUD) to those patients in violation of the medical standard of care. Compl. ¶¶ 6, 10.

The Court’s “class-certification analysis must be ‘rigorous’ and may ‘entail some overlap with the merits of the [Plaintiffs’] underlying claim,’” although this is not a “license to engage in free-ranging merits inquiries at the certification stage.” Amgen Inc. v. Connecticut Ret. Plans & Tr. Funds, 568 U.S. 455, 465-66 (2013) (quoting Wal-Mart Stores, Inc. v. Dukes, 564 U.S. 338, 351 (2011)). “Merits questions may be considered to the extent—but only to the extent—that they are relevant to determining whether the Rule 23 prerequisites for class certification are satisfied.” Id. A brief discussion of the merits and the evidence already developed in this case is necessary before the Court evaluates Rule 23 prerequisites. I. Wexford’s Guidelines on OUD and MOUD Plaintiffs initiated this action on July 7, 2023. Compl. at 43. Plaintiffs seek to certify two

classes: a forward-looking Injunctive Relief Class and a backward-looking Damages Class. The Damages Class looks back to July 2021. Until September 2022, Wexford had a policy of supervised withdrawal for patients with OUD. Pls.’ Ex. 7 (Mitcheff Dep.) at 170-71. Wexford’s 2022 guidelines explained the difference between this protocol and MOUD treatment: “Medically supervised opioid withdrawal should NOT be confused with medications for opioid use disorders (MOUD). Medically supervised opioid withdrawal involves treatment of withdrawal symptoms with medications usually over a short period of time while MOUD is a maintenance treatment of opioid use disorders.” Pls.’ Ex. 11 (2022 Medical Guidelines) at 29. MOUD does not only lessen withdrawal symptoms. As discussed below, MOUD has long-term benefits such as reducing “cravings that can result in return to [drug] use, overdose and overdose death.” Pls.’ Ex. 12 (2024 Medical Guidelines) at 35. Providers were directed to monitor patients using the Clinical Opiate Withdrawal Scale (COWS), which scores the severity of withdrawal based on gastrointestinal upset, tremors, anxiety,

bone or joint aches, tears, dilation of pupils, restlessness, sweating, and other symptoms. Pls.’ Ex. 10 (2017 Medical Guidelines) at 13, 18. Wexford’s director of addiction medicine, Dr. Michael Mitcheff, testified that providers treated symptoms with “Tylenol, ibuprofen, anti-diarrheal agent, anti-nausea vomiting agent, something to help [patients] sleep, [and] Clonidine to help with some of the symptoms.” Mitcheff Dep. at 176. The policy had one major exception: Pregnant women received MOUD treatment “ASAP” to prevent withdrawal. Pls.’ Ex. 10 (2017 Medical Guidelines) at 13; Mitcheff Dep. at 177-78; see also Pls.’ Ex. 11 (2022 Medical Guidelines) at 10 (explaining that withdrawal may result in miscarriage, stillbirth, or pre-term labor). Wexford issued Medically Supervised Withdrawal Guidelines in September 2022. See Pls.’ Ex. 11 (2022 Medical Guidelines). This policy recognized that patients dependent on opioids

“experience particularly intense withdrawal symptoms” for five to seven days, and “post-acute withdrawal syndrome (PAWS) can last over a year.” Id. at 11. Primary treatment considerations were: “Symptomatic medications such as Clonidine, Zofran, Tylenol and Imodium AD.” Id. at 13. The policy encouraged MOUD “if a patient comes in on this treatment” and for new patients with OUD “if acceptable to client leadership.” Id. at 11. The guidelines advised that opioid withdrawal “results in significant symptomatology, which can be markedly reduced with targeted therapies or prevented with continuation or initiation of medications for opioid use disorder (MOUD).” Id. at 30. The 2022 guidelines included comparisons of four types of MOUD treatment: buprenorphine, buprenorphine/naloxone, methadone, and naltrexone. Id. at 79-80. The Food and Drug Administration (FDA) has approved three medications to treat OUD: buprenorphine, methadone, and naltrexone. Information about Medications for Opioid Use Disorder (MOUD), FDA (Dec. 26, 2024), https://perma.cc/6HCU-BU9U. Buprenorphine/naloxone formulations contain naloxone to prevent abuse. What are the treatments

for heroin use disorder?, National Institutes of Health (April 13, 2021), https://perma.cc/F9HL- VBD9. Wexford updated its guidelines again during the pendency of this action. The 2024 policy “encourages continuation of MOUD if a patient comes in on this treatment” and recommends that patients with OUD “should be offered MOUD and not taken through the full withdrawal process unless the patient prefers using Naltrexone, or prefers abstinence.” Pls.’ Ex. 12 (2024 Medical Guidelines) at 13. The policy further provides that clinicians may provide “clinically appropriate medically supervised withdrawal” where MOUD is not available “based on facility rules.” Id. On the next line, the policy states in bold text: “If a patient needs to go through medically supervised withdrawal, a tapering dosage of buprenorphine is recommended to treat the withdrawal.” Id.; see

also Mitcheff Dep. at 174 (explaining that in some facilities providers use buprenorphine to make withdrawal “smoother” and “much less symptomatic”). Primary treatment considerations were: “If actively addicted, transition onto buprenorphine then taper off gradually (if unable or unwilling to stay on transmucosal buprenorphine)” and “Symptomatic medications such as Clonidine, Zofran, Tylenol and Imodium AD.” Pls.’ Ex. 12 (2024 Medical Guidelines) at 15. In a section titled “Opioid Withdrawal,” the guidelines state: It should be noted that Wexford recommends a comprehensive MOUD program that includes all three FDA-approved medications but we also understand that we are required to follow the client’s policies. . . . It is Wexford Health’s recommendation that consideration be given to initiating ongoing treatment for OUD with buprenorphine. This will prevent severe opioid withdrawal, help with cravings that can result in return to use, overdose and overdose death. Id. at 35. Wexford concedes that MOUD is an appropriate treatment for OUD and often the best treatment for patients with OUD. Def.’s Resp. at 1.

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