HENRY E. HUDSON, District Judge.
Plaintiff Ricky Jovan Gray, a Virginia state inmate sentenced to death, brings this civil rights action under 42 U.S.C. § 1983. Gray is currently scheduled to be executed by lethal injection on January 18, 2017, a date that was set on November 21, 2016. On December 14, 2016, Gray filed this Complaint for Declaratory Judgment, and on December 16, 2016, he filed this Emergency Motion for Temporary Restraining Order and Preliminary Injunction.
Gray alleges that "[t]here is a constitutionally intolerable risk that, on January 18, 2017, the Virginia Department of Corrections ("VDOC") will chemically torture [him] to death" and that "[t]he VDOC will do so behind a veil of secrecy that frustrates Mr. Gray's efforts to learn any meaningful details about the chemicals that will be used to cause his death." (Compl. ¶ 1, ECF No. 1.) Gray contends that "[t]he risk of chemical torture is in violation of [his] Eighth Amendment right to be free from cruel punishment" and that "[t]he veil of secrecy that the VDOC has pulled across the details surrounding how Mr. Gray is to be executed is a violation of Mr. Gray's Fifth and Fourteenth Amendment right to Procedural Due Process." (Id.) Specifically, Gray speculates that the compounded midazolam that the VDOC intends to use as the first drug in its three-drug protocol will not sufficiently anesthetize him before the administration of the second- and third-stage drugs. Gray also challenges Virginia's plan to use a second compounded drug in the third stage of the lethal injection protocol.
The Court's central focuses are Gray's Motion for Preliminary Injunction and Defendants' Opposition thereto. On January 3, 2017, the Court heard evidence and oral argument on the Motion for Preliminary Injunction. For the reasons set forth below, Gray's Motion will be denied.
It has been eleven years since Gray brutally murdered Kathryn and Bryan Harvey and their two young daughters, Stella and Ruby, on New Year's Day, 2006. A Virginia jury convicted Gray of five counts of capital murder and sentenced him to death on two of the counts, the murders of Stella and Ruby Harvey. Since then, Gray has unsuccessfully pursued a host of direct and post-conviction challenges and appeals in both state and federal courts. On October 3, 2016, the United States Supreme Court denied Gray's petition for a writ of certiorari challenging his convictions and death sentences. Gray v. Zook, 137 S.Ct. 84 (2016). Faced with his impending execution, Gray filed the instant challenge.
The Supreme Court of Virginia aptly summarized the undisputed evidence of his guilt as follows:
Gray v. Commonwealth, 645 S.E.2d 448, 452-54 (Va. 2007) (alterations in original).
During the sentencing phase of his criminal proceedings, "[e]xtensive evidence was also presented to show a history of violent acts perpetrated by Gray." Id. at 454.
Id. at 454-55.
Gray contends that "this Court should temporarily and preliminarily enjoin Defendants from executing Mr. Gray on January 18, 2017, and order that Mr. Gray may take discovery—including discovery that may reveal the identity of the compounding pharmacy that prepared th[e] compounded midazolam and compounded potassium chloride at issue in this matter. . . ." (Br. Supp. Mot. Prelim. Inj. 30, ECF No. 14.) Gray claims that midazolam "presents a host of serious risks" (Id. at 9), because while it "can render inmates initially unconscious, it cannot produce and maintain anesthesia." (Id. at 7-8 (footnote omitted).) Gray argues that the VDOC's planned use of compounded drugs, including compounded midazolam, carries a demonstrated risk of inflicting severe pain upon him. (Id. at 9-13.) Gray contends that using midazolam and potassium chloride prepared by a compounding pharmacy "adds an additional layer of intolerable risk" because, "[u]nlike ordinary pharmaceutical manufacturers, non-traditional compounding pharmacies are not subject to federal Good Manufacturing Practice Guidelines and FDA oversight." (Id. at 10 (citation omitted).)
Gray argues that "[i]t is nearly impossible to verify the quality of [the raw ingredients, called Active Pharmaceutical Ingredients ("APIs"),] used in compounding" (Id.), which "create[s] a significant risk that compounded preparations will not be pharmacologically similar to the FDA-approved drugs they imitate." (Id. at 11.) Gray also cites concerns about mislabeling and the risk of contamination during the manufacturing process. (Id. at 11-12.)
Gray notes that high-risk sterile drugs like midazolam and potassium chloride would have a maximum beyond use date ("BUD") of 24 hours if stored at room temperature, 72 hours if refrigerated, and 45 days if frozen. (Id. at 12.) Gray explains that "[t]he bottles holding the purported compounded midazolam and compounded potassium chloride supplied by the VDOC have labels suggesting that the `projected expiration dates' (not the BUD) are in February and May of 2017." (Id. (citation omitted).) Gray contends that "[t]he VDOC has not provided any evidence to support this as a BUD, and for the reasons noted above, it is unlikely that these compounded drugs will remain stable and effective over this period of time." (Id. at 12-13.) Finally, Gray identifies three instances where compounded pentobarbital, which is not a drug that the VDOC intends to use here, allegedly caused problems in an execution. (Id. at 13-14.)
Gray also contends that because he suffered "severe and protracted sexual abuse," he now "faces terrifying nightmares in which Mr. Gray continues to experience himself as a child, being raped." (Id. at 14; see also Lisak Decl. ¶¶ 13-14, ECF No. 17.) According to Gray and his expert, Dr. Lisak, the VDOC's lethal injection protocol "will cause Mr. Gray extreme terror, and play upon one of Mr. Gray's most significant and longstanding fears" of being paralyzed. (Br. Supp. Mot. Prelim. Inj. 15 (citing Lisak Decl. ¶ 16).) Dr. Lisak speculates that, based on Gray's description of his nightmares where he cannot move his legs or arms, Gray experiences "tonic immobility." (Lisak Decl. ¶ 14.) Dr. Lisak also states that "Gray exhibits many symptoms of Post-Traumatic Stress Disorder." (Id. ¶ 15.) According to Gray, he "will therefore experience the psychological torture from his nightmare of being harmed while immobilized, a personalized torment that counsels in favor of an alternative method of execution." (Br. Supp. Mot. Prelim. Inj. 15.)
Gray argues that the VDOC has at least one alternative to the three-drug lethal injection protocol. He alleges that electrocution, in the legal sense, is not a known and available alternative because it is unconstitutional, and instead proposes a firing squad.
Finally, Gray argues that he "has been stymied in his attempts to learn any [of a host of purportedly] critical facts about the efficacy of drugs that the VDOC intends to use to execute him" by Virginia's "Secrecy Statute," contained in section 53.1-234 of the Code of Virginia ("Secrecy Statute"). (Id. at 24.) That statute states in pertinent part:
Va. Code Ann. § 53.1-234. Gray alleges that the Secrecy Statute is unconstitutional or, in the alternative "does not apply in this federal court proceeding adjudicating federal rights." (Id. at 25.)
The Court has considered the evidence presented by the parties and the testimony received during the evidentiary hearing, and as discussed below, finds that Gray falls far short of demonstrating entitlement to a preliminary injunction.
Gray produced three witnesses in support of his Motion for Preliminary Injunction and Temporary Restraining Order.
The Commonwealth called four witnesses to address the issues raised by Gray. Dr. Daniel Buffington, an expert in clinical pharmacology and toxicology described the efficacy of 500 mg of midazolam as the first-drug in the three-drug protocol. (See generally id. at 46-80.) A. David Robinson, the Chief of Corrections Operations for the VDOC, recounted the difficulty encountered by the VDOC in acquiring lethal injection drugs. He also explained the methodology the VDOC has employed for monitoring and controlling the potency of the compounded drugs at issue. (See generally id. at 87-109.) Dr. Frank Fuller, a VDOC pharmacist, detailed the procedure for storage and potency monitoring of the compounded drugs at issue. (See generally id. at 129-46.) Finally, Shane Wyatt, a chemist at the Virginia Department of Consolidated Laboratory Services, General Services Division ("VDCL"), described the tests he conducted on the compounded midazolam and compounded potassium chloride designated for use in this case, to ensure the integrity and continued potency of the drugs. (See generally id. at 155-68.)
Initially, the Court notes an absence of expert testimony quantifying the risk Gray actually faces in the current execution scheme.
As an alternative to execution by electric chair, Virginia adopted lethal injection on January 1, 1995. Since then, Virginia has successfully executed 80 inmates by lethal injection. Virginia employs a three-drug protocol to perform an execution by lethal injection. (VDOC Operating Procedure 460 at 10-11, ECF No. 21-1.) Clearly, this method of execution was used by Virginia long before Gray committed the violent murders of the Harvey family in 2006. Virginia has also employed a three-drug protocol during the ensuing eleven years while Gray has been challenging his convictions and death sentence.
The first drug in Virginia's protocol renders the condemned inmate unconscious. As has been alleged in prior cases, see, e.g., Prieto v. Clarke, No. 3:15CV587-HEH, 2015 WL 5793903, at *1 (E.D. Va. Oct. 1, 2015); Reid v. Johnson, 333 F.Supp.2d 543, 551 (E.D. Va. 2004), Gray primarily speculates that the first drug in Virginia's protocol may be ineffective, subjecting him to intolerable pain from the administration of the second and third drugs.
In light of the pressure waged by death penalty opponents, it has become increasingly difficult to obtain the drugs Virginia traditionally used to render a prisoner unconscious during the initial stage of the execution process. For this reason, in recent years the VDOC has approved the use of midazolam and pentobarbital as permissible first-stage drugs in the protocol. Robinson explained that the VDOC has encountered difficulty obtaining either of these drugs from its traditional suppliers. (Prelim. Inj. Hr'g Tr. 91.) He testified that for the last Virginia execution, the VDOC had to obtain compounded pentobarbital from Texas as its first drug in the three-drug protocol. (Id. at 92.) Robinson noted that if Texas had not supplied the VDOC with the compounded pentobarbital, the VDOC had no other available source to acquire the necessary drugs for that execution. (Id.) Robinson attempted to obtain pentobarbital and sodium thiopental for Plaintiffs execution, but no pharmacy would supply him with these drugs. (Id. at 99.) Because death penalty opponents have made it difficult to obtain FDA-approved drugs customarily used in executions, Virginia has recently resorted to obtaining drugs from compounding pharmacies instead of traditional suppliers.
Robinson explained that after passage of the Secrecy Statute, the VDOC spoke with twenty to twenty-five pharmacies in Virginia about obtaining lethal injection drugs. (Id. at 93.) The VDOC was required to enter into a Memorandum of Understanding with a compounding pharmacy before the pharmacy agreed to provide the VDOC with the necessary drugs. (ECF No. 21-2.) Total confidentiality about the pharmacy's identity was an essential term of that agreement. (Prelim. Inj. Hr'g Tr. 95.)
By October 6, 2016,
(Br. Supp. Mot. Prelim. Inj. 3.) The VDOC obtained two batches of compounded midazolam and compounded potassium chloride from the compounding pharmacy. Robinson himself picked up both of these batches of drugs. (Prelim. Inj. Hr'g Tr. 96.) The VDOC has certified that the compounded drugs were prepared between August 1 and October 31, 2016, by a pharmacy that is licensed to operate in Virginia under the direction of a licensed pharmacist. (ECF No. 15-6, at 4.) Proper chain of custody was maintained at all times, and the transfers were accomplished in accordance with instructions from the licensed pharmacist. (Id.) Dr. Fuller indicated that he received the batches of compounded drugs and stored the drugs under manufacturer-required temperatures. (Prelim. Inj. Hr'g Tr. 130.) Dr. Fuller and the compounding pharmacist who made the drugs agreed that they should be stored at room temperature in order to prevent potential precipitate, which would render the drugs unsuitable for injection. (Id. at 131.) Dr. Fuller inspected the drugs and confirmed that they had no visible precipitate, were not cloudy, and that their bottles were sealed. (Id. at 132-34.)
For the first batch, the label for the bottle containing midazolam indicated that the "projected expiration date" was April 1, 2017 (ECF No. 21-3, at 1-3), and the label for the first bottle containing compounded potassium chloride stated that the "projected expiration date" was February 28, 2017 (ECF No. 21-4, at 1). Dr. Fuller explained that these bottles were not labeled with BUDs, in part, because the VDOC intended to test the drugs monthly to determine whether the drugs had deteriorated, alleviating the need for beyond use dates.
On October 26, 2016, Shane Wyatt received "two sealed containers," one of potassium chloride, and one of midazolam, that were tested for "[verification of labeled concentration for each container." (ECF No. 21-5, at 1.)
Robinson testified that the VDOC later obtained a second batch of drugs from the compounding pharmacy containing one bottle of compounded midazolam and one bottle of compounded potassium chloride. (Prelim. Inj. Hr'g Tr. 97.) For the second batch, the label for the bottle containing midazolam indicated that "projected expiration date" was May 1, 2017 (ECF No. 21-7), and the label for the bottle containing compounded potassium chloride stated that the "projected expiration date" was May 1, 2017 (ECF No. 21-8). The VDOC sent this second batch, along with the initial batch that had already been tested, to the VDCL for testing. On December 5, 2016, Wyatt received "four sealed containers," two of potassium chloride and two of midazolam, that were tested for "[v]erification of labeled concentration for each container." (ECF No. 21-6, at 1.) The label for the previously tested potassium chloride stated that it was 250 mL of 2 mEq/mL potassium chloride, and the VDCL's second test reflected that the compounded potassium chloride had a concentration of 1.98 plus or minus 0.006mEq/ML Chloride and 2.05 plus or minus 0.020 mEq/mL Potassium. (Id.) The new bottle of potassium chloride was labeled as 250 ML of 2 mEq/mL, and the VDCL's test reflected that it contained 1.99 plus or minus 0.006 mEq/mL Potassium and 2.08 plus or minus .020 mEq/mL Potassium. (Id.) The label for the previously tested midazolam stated that its concentration was 10 mL of 5 mg/mL midazolam, and the VDCL's second test reflected that the compounded midazolam was 5.07 plus or minus 0.77 mg/mL midazolam. (Id.) The label for the second bottle of midazolam indicated that it contained 10 mL of 5 mg/mL midazolam, and the VDCL's test reflected that the concentration was 5.00 plus or minus .077 mg/mL midazolam. (Id.) Dr. Fuller testified that the tests demonstrated that the concentrations were consistent both with their labels and with their commercially manufactured counterparts. (Prelim. Inj. Hr'g Tr. 136.) Wyatt confirmed that the tests matched the bottles' labeled concentrations. (Id. at 163.)
Wyatt testified that he conducted a full scan on these bottles for total concentration and to confirm the identity of the contents. (Id. at 156.) He inspected all four bottles of compounded drugs for any cloudiness or precipitate and noted that the substances appeared clear. (Id. at 163.) Wyatt testified that his lab does not test for sterility or endotoxins. (Id. at 164.) He explained, however, that any impurities or other substances mixed in the compound would have resulted in a greater presence of spikes on the graph created by the mass spectrometer than what he observed.
The VDOC will use 500 mg of midazolam as its first-stage drug in the three-drug lethal injection protocol. Midazolam is used as a sedative. It is a central nervous system and respiratory depressant. Dr. Sasich, Dr. Buffington, and Dr. Groner all agreed that much smaller amounts of midazolam are used for medicinal or therapeutic purposes. Midazolam is "dose dependent," meaning that the more an individual is administered, the greater the effect will be, leading to more progressive levels of sedation. Five milligrams is considered a high dosage for medicinal or clinical use. Doses as small as 10 mg to 20 mg have resulted in death. Dr. Buffington explained that "[t]here would be absolutely no therapeutic utility or rationale to use" 500 mg of midazolam "for a clinical purpose." (Prelim. Inj. Hr'g Tr. 54.) Dr. Buffington noted that administration of 500 mg of midazolam would result in "respiratory failure" and a "certainty of death." (Id. at 52, 54.) He further explained that there is no data to support the idea that midazolam has a so-called ceiling effect. (Id. at 55, 69.)
Dr. Buffington agreed that midazolam is neither approved by the FDA or other medical licensing agencies for use as a general anesthetic, nor is it indicated in reference books for that purpose. (Id. at 61, 64.) He explained that midazolam would not be used alone during a clinical procedure to induce general anesthesia because of its significant, life-threatening, adverse side effects at the doses that would be required. (Id. at 61, 66.) Dr. Buffington explained that at higher doses midazolam causes life-threatening respiratory depression, "which is consistent with the desired application in this particular case." (Id. at 62.)
Dr. Buffington also explained that he would not expect that a patient would be conscious during depression of respiratory symptoms, because "if you're going to say that the drug is having one effect, you would expect it to have all the effects. So if you've got a serious profound respiratory depression, you've also got serious sedation and significant anesthetic effects all simultaneous. So, I would not expect the respiratory depression effect to be something the person would be cognizant of." (Id. at 63.) Because midazolam suppresses the respiratory system, any signs of respiratory distress such as coughing or gasping would be normal reflexes of respiratory distress, but these signs do not mean the person is conscious. (Id. at 70.)
Dr. Buffington steadfastly confirmed that a dose of midazolam well below 500 milligrams "would render an individual unconscious with anterograde amnesia and insensitive to noxious stimuli." (Id. at 55.)
Dr. Buffington explained that drugs are compounded "routinely" and that compounded drugs are as efficacious as their commercially manufactured counterparts. (Id. at 50.) Robinson testified that the VDOC obtained the compounded midazolam and compounded potassium chloride from a licensed pharmacy and that the compounds were made by a licensed pharmacist. (Id. at 94.) The compounding pharmacy selected by the VDOC had no FDA or Virginia Department of Pharmacy regulatory infractions. (Id.) While Gray's expert espouses a host of hypothetical risks that could result from a compounding pharmacy's preparation of drugs, Dr. Buffington rejoined that he would have confidence in the integrity of compounded drugs made in a licensed pharmacy, that the drugs would be sterile, and that the pharmacy prepared the drugs correctly and in compliance with appropriate standards. (Id. at 74-76.) Dr. Buffington noted that the FDA or state boards of pharmacy do not set standards for execution drugs. (See id. at 59.) He also explained that concerns about drug preparation, storage, and compliance with beyond use dates are concerns for clinical applications, to avoid potential harm patients, not for correctional applications. (See id. at 71, 73-74.) He explained that for corrections applications, drugs are used for their adverse side effect; "the end goal of the combined administration of these medications is worse than any potential adverse side effect" from improper storage. (Id. at 73-74.)
Robinson testified that he has worked for the VDOC for thirty-five years and has observed thirteen executions. (Id. at 88.) The execution team practices once a month, regardless of whether an execution is scheduled. (Id.) When an execution date has been set, the team practices twice a month and once a week within a month of the execution. (Id.) Robinson explained that the team simulates the process by conducting a "dry-run" of both the electric chair and lethal injection protocols. (Id. at 89.) A consciousness test is an integral part of that regimen. (Id.) This consciousness test ensures that the individual has no reaction to noxious stimuli. (Id. at 89-90.) Robinson explained that two experienced medical professionals, who have participated in prior executions, are a part of the team and ensure the proper insertion of the IV. (Id. at 90.) Robinson testified that in the VDOC's execution of Alfredo Prieto in October 2015, a compounded drug, pentobarbital, was the first drug administered in the three-drug lethal injection. (Id. at 92-93.) Robinson observed that execution and noted that there were no complications. (Id. at 93.)
Dr. Groner testified that, in his opinion, execution by firing squad would result in "nearly instantaneous and painless" death. (Groner Decl. ¶ 7, ECF No. 18.) According to Utah's protocol, the firing squad would aim at a target placed over the individual's heart. (Id. ¶ 9.) A properly aimed bullet would tear the left ventricle, causing cessation of the blood to the brain, resulting in unconsciousness within seconds. Death would follow within three to four minutes. (Id. ¶ 10.) Dr. Groner agreed that an individual would be conscious when the bullet hit his chest. (Prelim. Inj. Hr'g Tr. 120.) Dr. Groner admitted that he could not quantify with any degree of certainty how much pain an individual would experience. (Id. at 120-21.) Dr. Groner also admitted that if the bullet missed the target, the individual "could suffer" and would experience an "agonizing death." (Id. at 121.) Dr. Groner, however, offered no convincing testimony as to why being shot could not be extremely painful.
Moreover, Robinson testified that the VDOC could not carry out an execution by firing squad. Because VDOC employees have not been trained in that methodology, the VDOC does not have a chamber in which to conduct such an execution, and the VDOC has not explored the cost of such a procedure. (Id. at 99-100.) Robinson explained that the VDOC is not authorized to use a manner of execution that has not been approved by the Virginia General Assembly. (Id. at 100.)
"A plaintiff seeking a preliminary injunction must establish that he is likely to succeed on the merits, that he is likely to suffer irreparable harm in the absence of preliminary relief, that the balance of equities tips in his favor, and that an injunction is in the public interest." Glossip v. Gross, 135 S.Ct. 2726, 2736-37 (2015) (quoting Winter v. Nat. Res. Def. Council Inc., 555 U.S. 7, 20 (2008)). The Fourth Circuit Court of Appeals has clearly articulated an analytical framework for applying the teachings of Winter. See Real Truth About Obama, Inc. v. Federal Election Commission, 575 F.3d 342, 346-47 (4th Cir. 2009), vacated on other grounds, 559 U.S. 1089 (2010). Gray, as the party seeking a preliminary injunction, bears the burden of establishing that each factor supports granting the injunction. Real Truth, 575 F.3d at 346. Each factor must be demonstrated by a "clear showing." Winter, 555 U.S. at 22. Failure to satisfy any one of the relevant factors mandates denial of the preliminary injunction. Real Truth, 575 F.3d at 346. As explained below, Gray fails on all four fronts.
The Supreme Court has emphasized that "because it is settled that capital punishment is constitutional, `[i]t necessarily follows that there must be a [constitutional] means of carrying it out.'" Glossip v. Gross, 135 S.Ct. 2726, 2732-33 (2015) (alterations in original) (quoting Baze v. Rees, 553 U.S. 35, 47 (2008)). Because "[s]ome risk of pain is inherent in any method of execution—no matter how humane," the Eighth Amendment "does not demand the avoidance of all risk of pain in carrying out executions." Baze, 553 U.S. at 47. More specifically, "[s]imply because an execution method may result in pain, either by accident or as an inescapable consequence of death, does not establish the sort of `objectively intolerable risk of harm' that qualifies as cruel and unusual." Id. at 50. As another district court has astutely noted: "The pharmaceutical manufacturers' withdrawal of the best drugs from use in executions does not end capital punishment." First Amendment Coal, of Az. v. Ryan, ___ F. Supp. 3d ___, 2016 WL 2893413, at *5 (D. Az. May 18, 2016).
"[Prisoners cannot successfully challenge a method of execution unless they establish that the method presents a risk that is sure or very likely to cause serious illness and needless suffering, and give rise to sufficiently imminent dangers." Glossip, 135 S. Ct. at 2737 (internal quotation marks omitted) (quoting Baze, 553 U.S. at 50). "A stay of execution may not be granted on grounds such as those asserted here unless the condemned prisoner establishes that the State's lethal injection protocol creates a demonstrated risk of severe pain." Id. (quoting Baze, 553 U.S. at 61). The inmate must also show that "the risk is substantial when compared to the known and available alternatives." Id. (quoting Baze, 553 U.S. at 61). The burden rests with Gray to "plead and prove" both prongs of the test. Id. at 2739; see Brooks v. Warden, Comm'r Ala. Dep't of Corr., 810 F.3d 812, 819 (11th Cir. 2016) (citation omitted), cert. denied, 136 S.Ct. 979 (2016).
The Supreme Court has rejected a similar Eighth Amendment challenge to the three-drug protocol that the VDOC will use here to execute Gray. Glossip, 135 S. Ct. at 2737-38 (affirming district court's denial of preliminary injunction because inmate failed to establish that the use of midazolam was sure or very likely to cause needless suffering). Although Gray makes much of the fact that the VDOC will use compounded midazolam, he fails to demonstrate that compounded midazolam is pharmacologically inferior to non-compounded midazolam. In fact, persuasive evidence in the case at hand is to the contrary.
Initially, Gray argues that midazolam "is not an anesthetic at all" (Br. Supp. Mot. Prelim. Inj. 1), and that "midazolam in any form is wholly unsuited to the task of anesthetizing [him]" (Id. at 6), because it "poses a recognized and substantial risk of causing [him] severe pain." (Id.) Gray supports his arguments with the following contentions: (1) midazolam is an anxiety medicine, and while it "can render inmates initially unconscious, it cannot produce and maintain anesthesia" (Id. at 8-9 (footnote omitted)); (2) midazolam has a "ceiling effect" (Id.); (3) midazolam itself could cause Gray pain (Id); and, (4) three inmates who were executed using midazolam in 2014 and 2015 twitched or gasped for air. (Id. 8-9.)
The United States Supreme Court and several appellate courts have uniformly rejected challenges to lethal injection protocols that use midazolam as the first drug in a three-drug lethal injection protocol because the plaintiffs had not established that it poses a constitutionally unacceptable risk of pain. See Glossip, 135 S. Ct. at 2731; Grayson v. Warden, ___ F. App'x ___, 2016 WL 7118393, at *4-5 (11th Cir. Dec. 7, 2016) (explaining that "Supreme Court and `numerous other courts' have concluded that midazolam is an adequate substitute for pentobarbital as the first drug in a three-drug lethal injection protocol" (citing Brooks, 810 F.3d at 822-24))). Based on the evidence in the immediate case, the Court fails to discern any reason to conclude otherwise.
Gray acknowledges that the United States Supreme Court has categorically rejected each of these arguments. See Glossip, 135 S. Ct. at 2731; see also Brooks, 810 F.3d at 818-22 (rejecting similar arguments after Glossip). Nevertheless, counsel argues that the "Supreme Court has not `approved' the use of midazolam in three-drug protocol lethal-injection executions." (Br. Supp. Mot. Prelim. Inj. 7 n.4.) While the Court does not suggest that the Supreme Court has endorsed midazolam's constitutionality in all applications, Gray cannot ignore that in similar, if not identical, challenges to the use of the drug, the Supreme Court found those arguments unpersuasive and declined to order a stay of execution. See Glossip, 135 S. Ct. at 2726, 2740-44. The Supreme Court explicitly rejected Gray's arguments that midazolam could not maintain anesthesia and that midazolam had a "ceiling effect."
Indeed, the Supreme Court rejected the testimony of Gray's own witness, Dr. Sasich, that midazolam was "powerful enough to induce unconsciousness," but "too weak to maintain unconsciousness and insensitivity to pain." Id. at 2740-41. Instead, the Supreme Court found credible testimony that 500 mg of midazolam would render a person insensate to pain. Id. at 2741. The Supreme Court further found Dr. Sasich's theory about midazolam having a "`ceiling effect" when administered in high doses "speculative" and unconvincing. Id. at 2743-44. The Supreme Court also found no merit in the argument that midazolam itself can cause paradoxical reactions. Id. at 2740 n.3. Having weighed the testimony of Dr. Sasich and Dr. Buffington, the Court is firmly convinced that a 500 mg injection of midazolam would render a person insensate to pain. Dr. Sasich's testimony is inconsistent with the weight of credible authority.
The Supreme Court also rejected Gray's fourth argument, that "[Clayton] Lockett['s execution in Oklahoma] and Arizona's July 2014 execution of Joseph Wood establish that midazolam is sure or very sure to cause serious pain." Id. at 2745. The Supreme Court explained: "When all circumstances are considered, the Lockett and Wood executions have little probative value for the present purposes." (Id. at 2746.) The Court finds the same holds true here.
Counsel for Gray now adds that Ronald Bert Smith, executed in Alabama several weeks ago, "struggled for breath and heaved and coughed and clenched his left fist" after receiving the injection of midazolam. (Br. Supp. Mot. Prelim. Inj. 1 (internal quotation marks omitted) (citation omitted).) However, the fact that Smith struggled for breath, heaved, coughed, and clenched his fist, without more, falls far short of showing that midazolam "is sure or very likely to cause serious illness and needless suffering." Glossip, S. Ct. at 2737 (citation omitted); see also id. at 2733 (citation omitted) (recognizing that "some risk of pain is inherent in any method of execution" and "that the Constitution does not require the avoidance of all risk of pain").
Despite that fact that almost every argument advanced by Gray is contrary to settled Eighth Amendment jurisprudence, he has been afforded the opportunity to present evidence to support his allegations. See id. at 2740 (emphasis added) (explaining that "an inmate challenging a protocol bears the burden to show, based on evidence presented to the court, that there is a substantial risk of severe pain"). Even considering the subtle variances in Gray's contentions from those offered by the plaintiff in Glossip, he still fails to make any showing, much less a clear showing, that midazolam poses "an objectively intolerable risk of harm." Id. at 2737 (citing Baze, 553 U.S. at 50; see also id. at Glossip, 135 S. Ct. at 2740-46.
The evidence presented by Defendants establishes that the administration of 500 mg of midazolam can render a prisoner unconscious and insensate to pain during the remainder of the three-drug protocol. The evidence demonstrates that even 500 mg of midazolam used alone will result in a "certainty of death." (Prelim. Inj. Hr'g Tr. 54.)
Gray's allegations about a ceiling effect and the possibility that he could experience seizures or paradoxical effects are similarly conjectural. Gray's own witness acknowledged that there "might be" a ceiling effect, but it has never been empirically confirmed. (Id. at 36.) Dr. Buffington convincingly testified that the whole theoretical phenomenon of a ceiling effect with midazolam would be inconsequential because the individual would be deeply sedated prior to reaching that level. (Id. at 55-56.) Gray also puts forth no cogent evidence that he could experience seizures or "paradoxical reactions," or that those seizures or reactions in and of themselves indicate that the individual was experiencing needless suffering. See Warner v. Gross, 776 F.3d 721, 730, 732, 735-36 (10th Cir. 2016) (rejecting ceiling effect argument and paradoxical effects argument about midazolam as "speculative").
On this record, Gray fails to establish a substantial likelihood that Virginia's use of 500 mg of midazolam as the first drug in its lethal injection protocol "is sure or very likely to cause serious illness and needless suffering, and give rise to sufficiently imminent dangers." Glossip, 135 S. Ct. at 2737 (internal quotation marks omitted) (quoting Baze, 553 U.S. at 50); see Grayson, 2016 WL 7118393, at *5 (explaining that prior decisions about the use of midazolam "make it clear that it is not just unlikely that [Gray] will be able to make the showing required by the first prong of Glossip, but in fact it is virtually certain that he will be unable to do so"). Thus, he fails to demonstrate any likelihood of success on the merits with respect to his general challenge to midazolam as the first drug in the lethal injection protocol or that he is likely to suffer irreparable harm from its use.
Gray next contends that midazolam and potassium chloride prepared by a compounding pharmacy "adds an additional layer of intolerable risk." (Br. Supp. Mot. Prelim Inj. 6.) Again Gray fails to meet his burden of persuasion. Although he posits a list of potential hazards that may result from using compounded forms of midazolam and potassium chloride, he again fails to make any showing, much less a clear showing, that the drugs pose "an objectively intolerable risk of harm." Glossip, 135 S. Ct. at 2737 (internal quotation marks omitted) (quoting Baze, 553 U.S. at 50). Gray's attempt to suggest that the compounded drugs here are more dangerous than FDA-approved drugs is unsupported by the evidence.
The United States Court of Appeals for the Fifth Circuit recently rejected nearly identical arguments by a Texas death row inmate that "compounded drugs are unregulated and subject to quality and efficacy problems." Ladd v. Livingston, 777 F.3d 286, 289 (5th Cir. 2015); see also Wellons v. Comm'r, Ga. Dep't of Corr., 754 F.3d 1260, 1264-66 (11th Cir. 2014) (rejecting similar challenge to a compounded drug). The court concluded that such arguments are "essentially speculative," and "speculation cannot substitute for evidence that the use of the drug is sure or very likely to cause serious illness and needless suffering." Ladd, 777 F.3d at 289 (quoting Brewer v. Landigran, 562 U.S. 996, 996 (2010)). The Fifth Circuit explained that to succeed, an inmate must "offer some proof that the state's own process—that its choice of pharmacy, that its lab results, that the training of its executioners, and so forth, are suspect." Id. (citing Whitaker v. Livingston, 732 F.3d 465, 468 (5th Cir. 2013)). The court went on to observe that Texas was able to conduct its last fourteen executions with "a single-drug pentobarbital injection from a compounded pharmacy . . . without significant incident." Id. at 290. This Court previously refused to halt the execution of a Virginia inmate, Alfredo Prieto, whose lethal injection protocol used a compounded drug as its first ingredient. See Prieto v. Clarke, No. 3:15CV587-HEH, 2015 WL 5793903 (E.D. Va. Oct. 1, 2015). Prieto's execution using the compounded drug was completed without incident.
Gray and his expert, Dr. Sasich, question whether a compounding pharmacy could maintain the optimal standards necessary to produce midazolam that would retain its effectiveness for the period of time represented on the midazolam bottle. That disbelief, however, fails to substitute for persuasive evidence.
Gray and Sasich recounted a number of possible problems that could conceivably occur during the compounding process, including contamination and not maintaining the compounded drugs or their ingredients in the appropriate conditions. Again, this mere "speculation cannot substitute for evidence that the use of the drug is sure or very likely to cause serious illness and needless suffering." Ladd, 777 F.3d at 289 (quoting Brewer, 562 U.S. at 996). Gray has identified no deficiencies in Virginia's procurement of the drugs in question that would support a viable Eighth Amendment claim. See id. (citing Whitaker, 732 F.3d at 468). Hypotheticals are not sufficient to warrant a stay. See id., 777 F.3d at 289.
To the contrary, the evidence before the Court reflects that the VDOC selected a licensed pharmacy and a licensed pharmacist to make the compounded drugs. Moreover, the compounded midazolam and potassium chloride have been tested by the VDCL. The testing confirms that each bottle contains the substance and concentration that each label reflects and that the substance meets the concentration level of comparable manufactured drugs. The presence of contaminants in the compounded drugs would have been revealed in the VDCL's test results. Compounded drugs are utilized routinely, even in clinical settings, and are just as efficacious as their manufactured counterparts. Gray fails to point to any instance where a state has unsuccessfully used compounded midazolam or compounded potassium chloride in the execution context.
Gray also contends that high-risk drugs such as those at issue have BUDs of twenty-four hours at room temperature. He also points out that the high-risk drugs here are being maintained at room temperature but have expiration dates that far exceed twenty-four hours. Gray fails to supply any probative evidence that Virginia's maintenance of the drugs at room temperature or beyond twenty-four hours is "sure or very likely to cause serious illness and needless suffering." Glossip. 135 S. Ct. at 2737 (quoting Baze, 553 U.S. at 50). To the contrary, the VDOC tested the compounded drugs and found that they have retained their labeled concentration.
Simply put, Gray puts forth no evidence that compounded drugs subject him to "a substantial risk of serious harm." Id. (quoting Baze, 553 U.S. at 50). As such, Gray fails to a make a clear showing that he is likely to succeed on the merits or suffer irreparable harm.
Gray's challenge to the use of the three-drug lethal injection protocol also is premised on the allegation that its use will be unconstitutional as applied to him because he suffers from psychological issues that "would create particular fear and suffering relating to paralysis and unconsciousness." (Lisak Decl. ¶ 10, ECF No. 17.) Dr. Lisak speculates that Gray may have Posttraumatic Stress Disorder ("PTSD") based on Gray's statements that he suffers from nightmares in which he is paralyzed. Dr. Lisak proffers that the three-drug protocol's paralyzing effect may trigger Gray's PTSD-like symptoms. However, Dr. Lisak acknowledged that he had failed to address his concerns that Gray may have PTSD with the mental health professionals treating Gray at his place of incarceration. (Id. at 151.)
The evidence before the Court is wholly insufficient to demonstrate that Virginia's use of the three-drug lethal injection protocol creates a "substantial risk of serious harm" as applied to Gray. Dr. Lisak's testimony is entirely speculative and unpersuasive, as he fails to quantify the likelihood that Gray would experience constitutionally significant harm. See Arthur, 840 F.3d at 1309-12 (holding that as-applied challenge failed where inmate was unable to produce anything more than speculation that midazolam, as applied to him, would cause a heart attack before full sedation). The evidence before the Court "necessitates the conclusion that any estimation of what side effects are likely to occur and the severity of those side effects is wholly speculative." Coeey v. Strickland, 604 F.3d 939, 944 (6th Cir. 2010) (internal quotation marks omitted) (citation omitted). Speculation of this nature "cannot meet the standard of a sure or very likely risk of serious pain . . . that is substantial when compared to the known and available alternatives." Id. (internal quotation marks omitted) (citation omitted).
Alternatively, Gray fails to produce evidence that there are known and available alternatives that are feasible, readily implemented, and would significantly reduce a substantial risk of severe pain as applied to him. See Gissendaner v. Comm'r, Ga. Dep't of Corr. 779 F.3d 1275, 1283 (11th Cir. 2015) (finding fatal for the purposes of Fed. R. Civ. P. 12(b)(6) an inmate's failure to identify alternative method "that would substantially reduce the risks she identifies based on her gender, obesity, and possible sleep apnea"). As discussed below, the only available alternative that Gray offers is a firing squad, a method that is neither available nor likely to substantially reduce the risks Gray identifies based on his alleged psychological fear of being paralyzed.
In addition to the above failings, Gray is unlikely to succeed on the merits of his Eighth Amendment claim because he has failed to shoulder his responsibility to suggest an alternative method of execution that is "known and available" as well as "feasible, readily implemented, and in fact significantly [likely to] reduce a substantial risk of severe pain.'" Glossip, 135 S. Ct. at 2737 (quoting Baze, 553 U.S. at 52).
In an attempt to carry this substantial burden, Gray alleges that the Commonwealth "ha[s] refused to provide a constitutional execution method," and he proffers an alternative beyond Virginia's execution statute—the firing squad.
Gray's principal assertion that both of Virginia's statutorily provided methods of execution—lethal injection and electrocution—are unconstitutional contravenes settled precedent and is without merit. As an initial matter, Gray does not contend that lethal injection is per se unconstitutional. Instead, he merely challenges Virginia's current protocol. As discussed above, the Court finds that Gray is unlikely to prevail on his claim that the Commonwealth's proposed use of compounded midazolam and potassium chloride violates his Eighth Amendment right to be spared from cruel and unusual punishment. Moreover, the Court finds that Gray's argument that electrocution is unconstitutional defies over a century of settled case law to the contrary.
The Supreme Court first upheld electrocution as a constitutionally permissible method of execution in In re Kemmler, 136 U.S. 436, 447 (1890). Though the Court did not decide that case under the Eighth Amendment—instead analyzing the claim under the Fourteenth Amendment—In re Kemmler has been cited numerous times, both before and after the Eighth Amendment was incorporated against the states in Robinson v. California, 370 U.S. 660 (1962), for the proposition that electrocution remains a constitutional method of execution.
Gray argues through anecdotal accounts and the testimony of his expert witness, Dr. Groner, that the Court should reverse the polarity of the law by holding that electrocution violates the Eighth Amendment. As the Supreme Court has noted, its "decisions remain binding precedent until [it] see[s] fit to reconsider them, regardless of whether subsequent cases have raised doubts about their continuing vitality." Hohn v. United States, 524 U.S. 236, 252-53 (1998). The Supreme Court's decision in In re Kemmler and subsequent refusal to overrule it remains binding on this Court, and this Court lacks the authority to find otherwise.
Even if the Court were to re-assess the constitutionality of electrocution, it would find that Gray is not substantially likely to prevail on the merits of his claim. As the Supreme Court noted in Baze, "it is difficult to regard a practice as `objectively intolerable' when it is in fact widely tolerated." Baze, 553 U.S. at 53. Alabama, Arkansas, Florida, Kentucky, Oklahoma, South Carolina, Tennessee, Virginia, and the federal government have all statutorily authorized electrocution as a method of execution,
Moreover, Gray has failed to satisfy his burden of showing that he is likely to succeed on the merits of his claim that death by electrocution carries a "risk that is sure or very likely to cause serious illness and needless suffering." Glossip, 135 S. Ct. at 2737 (citation omitted). Gray's reference to eyewitness accounts only demonstrate that the physical effects of electrocution—namely burn marks, catching on fire, and smoke rising from the points of contact with the electrodes—may be visually disturbing to those witnessing the execution. (Br. Supp. Mot. Prelim. Inj. 15-17.) They do not provide evidence that the condemned inmates were conscious or able to feel these effects before dying. And Dr. Groner's testimony does not controvert this. Instead, he merely notes that "the evidence fails to show that inmates are rendered instantly senseless by the flow of electricity through the scalp electrode." (Groner Decl. ¶ 17.)
Because the Court finds that Gray is unlikely to satisfy the first prong of the Glossip analysis with respect to Virginia's lethal injection protocol and that, in the alternative, the Commonwealth has already provided him with a constitutionally "known and available" alternative method of execution by electrocution, the Court need not proceed in its analysis beyond the confines of Virginia's execution statute to consider a further alternative method of execution. Put succinctly, Virginia has provided Gray with two constitutional methods of execution. Gray is "not free to simply disregard those methods (and substitute his own) without satisfactorily establishing that those methods violate the constitutional command barring cruel and unusual punishment." Arthur, 840 F.3d at 1317. "Absent a showing that [the Commonwealth's] chosen methods of execution present an unconstitutional risk of severe pain, [Virginia] is under no obligation to deviate from its widely accepted, presumptively constitutional methods in favor of [Gray's] retrogressive alternative." Id. at 1318.
Nevertheless, as an alternative and independent ground, even if Gray had shown that he was likely to succeed on his Eighth Amendment claims as they pertain to lethal injection and electrocution, the Court would find that the firing squad is neither "feasible, readily implemented," nor "available" in Virginia. Glossip, 135 S. Ct. at 2737 (citations omitted).
It is undisputed that the firing squad is not currently a valid or lawful method of execution in the Commonwealth. See Va. Code Ann § 53.1-234. Therefore, a Virginia trial court "would be without any authority to order [Gray] to be executed by [that method]." Arthur, 840 F.3d at 1316. Additionally, the VDOC would be unable to carry out Gray's preferred death sentence without the General Assembly fundamentally rewriting its statute. Notwithstanding this, Gray argues that a method of execution need not be authorized by statute for it to be "feasible, readily implemented," or "available" under Glossip's second prong.
The Court disagrees and instead will join the panoply of courts that have confronted this issue in holding that a proposed alternative method of execution must be authorized by statute in order to be considered "available."
Moreover, Robinson testified that the firing squad has never been used in the Commonwealth of Virginia, that no correctional officers in the VDOC have been trained to carry out an execution by firing squad, and that no chamber currently exists where such an execution could take place. (Prelim. Inj. Hr'g Tr. 99-100.) Further, Virginia has not developed a protocol to carry out an execution by firing squad. While Gray has pointed to Utah's firing squad protocol as an exemplar, Virginia would not be bound to adopt an identical protocol if it chose to authorize this method of execution.
"[T]he reality is that formulating a new protocol and locating the people and resources necessary to carry out such an alternative . . . would take considerable time and would, inevitably, lead to an entire new round of legal challenges regarding the details of the protocols for constitutionally conducting an execution by firing squad." Arthur, 840 F.3d at 1319-20. The lack of currently available resources and inevitable delay that would accompany the implementation of a new method of execution necessarily undercut any potential argument that the firing squad is presently feasible or readily implemented.
Finally, even if the Court were to determine that the firing squad is a "known and available" as well as "feasible, [and] readily implemented" method of execution in Virginia, it would conclude that the method is not "significantly [likely to] reduce[] a substantial risk of severe pain." Glossip, 135 S. Ct. at 2737 (citations omitted). As discussed above, the Court finds that Gray has failed to demonstrate that he is likely to suffer from "severe pain" under Virginia's current lethal injection protocol. Consequently, he faces a high burden in attempting to demonstrate that the firing squad would somehow be a constitutionally superior method.
Gray's entire argument on this point is premised on Virginia's hypothetical adoption of an identical or similar protocol to the one used in Utah. (See Groner Decl. ¶ 9.) As previously noted, should Virginia choose to amend its execution statute and adopt the firing squad, the Commonwealth would be free to adopt whatever protocol it sees fit. This means that it could choose to adopt a substantially different procedure, including, but not limited to, requiring a different number of marksmen, a different caliber of ammunition, or a different location on the inmate's body at which to aim. A change in any one of these elements could have a drastic impact on the likelihood that human error would occur, which, by Dr. Groner's own testimony, could potentially result in an "agonizing" death.
Even if Virginia were to adopt Utah's firing squad protocol, the potential for human error still exists as the inmate could flinch or the executioners could miss their mark. There is no way for the Court to weigh a risk of human error in a not-yet-adopted firing squad protocol against any harm that Gray might face if the compounded midazolam does not render him fully unconscious and insensate. Consequently, Gray has not carried his burden of proposing an alternative method of execution that is "significantly [likely to] reduce a substantial risk of severe pain." Glossip, 135 S. Ct. at 2737 (quotations omitted) (emphasis added).
In view of the above, the Court concludes that Gray's failure to satisfy Glossip'§ second prong further supports a finding that he is unlikely to succeed on the merits of his Eighth Amendment claim.
As with his Eighth Amendment claim, Gray is also unlikely to succeed on the merits of his procedural due process claim. Gray contends that Virginia's Secrecy Statute, Va. Code Ann. § 53.1-234, is unconstitutional because it denies him access to information about Virginia's lethal injection drugs. Gray asserts that this is a violation of his procedural due process rights. However, this argument founders at the starting gate because no such right exists.
The constitutional right to procedural due process applies "only to the deprivation of interests encompassed by the Fourteenth Amendment's protection of liberty and property." Bd. of Regents of State Colleges v. Roth, 408 U.S. 564, 569 (1972). Thus, "the range of interests protected by procedural due process is not infinite." Wofford v. Evans, 390 F.3d 318, 325 (4th Cir. 2004) (quoting Bd. of Regents, 408 U.S. at 570). The United States Court of Appeals for the Fourth Circuit has never decided whether a death row inmate has a right to discover information pertaining to his execution.
Less than a year ago, the Eleventh Circuit held that a prisoner has no procedural due process right "to know where, how, and by whom the lethal injection drugs will be manufactured, as well as the qualifications of the person or persons who will manufacture the drugs, and who will place the catheters." Jones v. Comm'r, Ga. Dep't of Corr., 811 F.3d 1288, 1292-93 (11th Cir.), cert, denied sub nom. Jones v. Bryson, 136 S.Ct. 998 (2016). The Fifth, Sixth, and Eighth Circuits have reached similar conclusions. See Phillips v. DeWine, 841 F.3d 405, 420 (6th Cir. 2016) ("Plaintiffs argue that HB 663 prevents them from bringing an effective challenge to Ohio's execution procedures. Specifically, they maintain that HB 663 `denies [them] an opportunity to discover and litigate non-frivolous claims.' But no constitutional right exists to discover grievances or to litigate effectively once in court." (internal quotation marks omitted) (citation omitted)); Zink v. Lombardi, 783 F.3d 1089, 1109 (8th Cir.), cert, denied, 135 S.Ct. 2941 (2015) ("[T]he Constitution does not require such disclosure. A prisoner's assertion of necessity—that [the State] must disclose its protocol so he can challenge its conformity with the Eighth Amendment—does not substitute for the identification of a cognizable liberty interest." (internal quotation marks omitted) (citations omitted)); Trottie v. Livingston, 766 F.3d 450, 452 (5th Cir.), cert, denied, 135 S.Ct. 41 (2014) ("A due process right to disclosure requires an inmate to show a cognizable liberty interest in obtaining information about execution protocols. . . . However, we have held that an uncertainty as to the method of execution is not a cognizable liberty interest." (citation omitted)).
Gray also argues that the Court should stay his execution to provide time for discovery regarding his perceived Eighth Amendment claim. Gray requests that the Court order discovery to occur prior to the parties' initial Rule 26(f) conference pursuant to Fed. R. Civ. P. 26(d)(1). However, that request will be denied because, as discussed, Gray is unlikely to succeed on the merits of his underlying claims. As such, the Court is unwilling to delay Gray's execution so that he can embark on a fishing expedition. The Court, therefore, declines to address whether the privilege provided by Virginia's secrecy statute would hypothetically apply to this federal litigation.
Although the Court has devoted the majority of this opinion to addressing how Gray falls woefully short of demonstrating that he is likely to succeed on the merits of his claims or that he is likely to suffer irreparable harm, two additional factors firmly foreclose the availability of injunctive relief. Namely, Gray fails to make any showing that the balance of the equities favor him or that the public interest and equitable principles favor the grant of an injunction.
Evaluating the balance of equities requires the Court to assess the relative harm facing both parties. See E.I. DuPont de Nemours & Co. v. Kolon Ind., Inc., 894 F.Supp.2d 691, 708 (E.D. Va. 2012). Thus, on Gray's side of the scale is the possibility that he will experience some incremental discomfort and associated pain in his inevitable execution should the compounded midazolam fail to perform as expected.
Gray's potential harm is "a thin shadow compared to the certain, profound and [significant] harm to the state if an injunction is issued." Reid v. Johnson, 333 F.Supp.2d 543, 552 (E.D. Va. 2004). It is well settled that the state has "a significant interest in meting out a sentence of death in a timely fashion." Nelson v. Campbell, 541 U.S. 637, 644 (2004) (citing Calderon v. Thompson, 523 U.S. 538, 556-57 (1998); In re Blodgett, 502 U.S. 236, 238 (1992) (per curiam); McCleskey v. Zant, 499 U.S. 467, 491 (1991) ("[T]he power of a State to pass laws means little if the State cannot enforce them")). The state's interest in finality and in carrying out a sentence of death in a timely manner acquires "an added moral dimension" when the lengthy state and federal proceedings reviewing the conviction and sentence have run their course. Calderon, 523 U.S. at 556. At this point, the state and the victims of crime can expect the moral judgment of the state to be carried out without delay. Id. at 556 (citing Payne v. Tennessee, 501 U.S. 808 (1991)). "To unsettle these expectations is to inflict a profound injury to the powerful and legitimate interest in punishing the guilty, an interest shared by the State and the victims of crime alike." Id. (internal quotation marks omitted) (citations omitted). Here these harms are magnified by the appalling number of people, including two children ages four and nine, whom Gray tortured and killed. Accordingly, the balance of the equities firmly favors the Commonwealth.
This is not an instance where there are any questions as to innocence or sufficiency of due process of an individual set to be executed. Gray's "claim to receive a sentence of death without any unnecessary pain pales in comparison to the interest the general public has in the orderly administration of justice." Reid, 333 F.Supp.2d 543 at 553 (citing Calderon, 523 U.S. at 556-57). Thus, the Fourth Circuit has admonished that, "[l]ast minute stays [of execution] . . . represent an interference with the orderly processes of justice which should be avoided in all but the most extraordinary circumstances." Stockton v. Angelone, 70 F.3d 12, 13 (4th Cir. 1995) (per curiam). This is not such a case. The public interest in denying a stay rests firmly on the side of the Commonwealth.
Additionally, the Court must consider the timing and nature of Gray's request under general equitable principles. See Nelson, 541 U.S. at 649-50. In this respect, the Supreme Court instructed that courts should not countenance manipulation of the judicial process and emphasized that "there is a strong equitable presumption against the grant of a stay where a claim could have been brought at such a time as to allow consideration of the merits without requiring entry of a stay." Id. at 650.
Gray received two death sentences for the murders of Ruby and Stella Harvey on October 23, 2006, yet he waited until one month before his scheduled execution to bring a challenge to Virginia's method for carrying out his sentence. At the time Gray committed the horrific murders, Virginia used lethal injection as one method to execute those individuals sentenced to death. Moreover, ever since his 2006 sentencing, Gray was aware that Virginia would carry out that sentence either by electrocution or lethal injection. Gray's suggestion, that he could not have not challenged the method of his execution before October 2016, when he discovered that Virginia intended to perform his execution with compounded midazolam and potassium chloride, rings hollow. The difficulty states have faced in obtaining the appropriate drugs for conducting a lethal injection has been widely publicized and a topic of public debate for a number of years. Gray should have anticipated that Virginia might face similar problems in securing the drugs to execute him, particularly in the wake of an almost identical challenge in October 2015. See Prieto v. Clarke, No. 3:15CV587-HEH, 2015 WL 5793903 (E.D. Va. Oct. 1, 2015). Additionally, despite Gray's contention that he only learned that the state would use two compounded drugs in October, the underlying challenge to these two drugs is hardly novel. Gray fails to put forth any evidence that compounded drugs, in and of themselves, pose a risk that is "sure or very likely to cause serious illness and needless suffering." Glossip. 135 S. Ct. at 2737 (internal quotation marks omitted) (quoting Baze, 553 U.S. at 50).
If Gray acted with appropriate diligence, he would have had ample opportunity to address his concerns without disrupting the execution date set by the state court. By waiting as long as he did, Gray "leaves little doubt that the real purpose behind his claim is to seek a delay of his execution, not merely to effect an alteration in the manner in which it is carried out." Harris v. Johnson, 376 F.3d 414, 418 (5th Cir. 2004). Gray's delay in this matter is of significant magnitude and weighs heavily against him. See Gomez v. U.S. Dist. Ct. for the Northern Dist. of Cal, 503 U.S. 653, 653-54 (1992) (per curiam); Grayson v. Warden, Comm'r, Ala. Dep't of Corr., ___ F. App'x ___, 2016 WL 7118393, at *8 (11th Cir. 2016) ("While each death case is very important and deserves our most careful consideration, the fact that [the prisoner] has petitioned us for a stay of execution only at the very last moment, and without adequate explanation, also suggests to us that the equities do not lie in his favor." (quoting Jones v. Comm'r, Ga. Dep't of Corr., 811 F.3d 1288, 1297-98 (11th Cir. 2016))); Brooks v. Warden, Comm'r, Ala. Dep't of Corr., 810 F.3d 812, 825-26 (11th Cir. 2016).
The grant of interim injunctive relief is "an extraordinary remedy involving the exercise of a very far-reaching power, which is to be applied only in the limited circumstances which clearly demand it." Direx Israel, Ltd. v. Breakthrough Medical Corp., 952 F.2d 802, 811 (4th Cir. 1991) (internal quotation marks omitted). Each of the factors the Court must consider in granting such relief weigh decidedly and firmly against Gray. Accordingly, Plaintiffs Motion for Preliminary Injunctive Relief (ECF No. 13) will be denied. Plaintiffs Motion for a Temporary Restraining Order (ECF No. 12) will be denied as moot.
An appropriate Order will accompany this Memorandum Opinion.
(Id.)
Glossip, 135 S. Ct. at 2746 (internal citations omitted) (footnote omitted).