The Ninth Circuit denied Daniel Wayne Cook’s appeal for a stay of execution. There’s still the clemency hearing, but even if the Clemency Board recommends a stay, Governor Jan Brewer will veto it. So an execution is certain for April 5 - even though the prosecutor wouldn’t have sought the death penalty if he’d known all the facts.
Here is the Ninth Circuit’s opinion:
UNITED STATES COURT OF APPEALS
FOR THE NINTH CIRCUIT
DANIEL WAYNE COOK,
Plaintiff - Appellant,
JANICE K. BREWER; CHARLES L.
RYAN; ERNEST TRUJILLO; CARSON
MCWILLIAMS; DOES 1 - 50,
Defendants - Appellees.
D.C. No. 2:10-cv-02454-RCB
Appeal from the United States District Court
for the District of Arizona
Robert C. Broomfield, Senior District Judge, Presiding
Argued and Submitted March 10, 2011
Before: O’SCANNLAIN, GRABER, and CALLAHAN, Circuit Judges.
Opinion by Judge Callahan
CALLAHAN, Circuit Judge:
Plaintiff Daniel Wayne Cook (“Cook”), an Arizona prisoner scheduled for
execution on April 5, 2011, filed this action for equitable, injunctive and
MAR 16 2011
MOLLY C. DWYER, CLERK
U.S. COURT OF APPEALS
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Cook raised a third claim in his Complaint, that the State’s failure to
provide him with notice and information regarding the sodium thiopental that will
be used in his execution violates his Fourteenth Amendment rights, but he does not
challenge the district court’s decision on that claim in this appeal.
declaratory relief under 42 U.S.C. § 1983 (“§ 1983”) against Janice Brewer,
Governor of Arizona, as well as Charles Ryan, Ernest Trujillo, and Carson
McWilliams, who are Arizona Department of Corrections (“ADC”) officials
(collectively, “Defendants”). The district court granted Defendants’ motion to
dismiss for failure to state a claim upon which relief may be granted under Fed. R.
Civ. P. 12(b)(6) (“Rule 12(b)(6)”). On appeal, Cook challenges the district court’s
decisions regarding two of his Eighth Amendment claims.
First, he argues that
Defendants’ intent to use a foreign manufactured non-Food and Drug
Administration (“FDA”) approved substance (which Defendants state is sodium
thiopental) in his execution creates a substantial and unnecessary risk of
unconstitutional pain. Second, Cook contends that the administration of this
substance by medical professionals would constitute deliberate indifference to his
right to be free from cruel and unusual punishment. We affirm.
Cook is scheduled for execution on April 5, 2011, for his role in two 1987
murders in Lake Havasu City, Arizona. State v. Cook, 821 P.2d 731, 738 (Ariz.
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1991). Cook and his roommate tortured, sodomized and killed Carlos Cruz Ramos
and Kevin Swaney. Id. at 736–37. A jury thereafter convicted him of two counts
of first-degree murder and the court sentenced him to death under Arizona Revised
Statutes §§ 13-503 and 13-703. Id. at 737–38.
After the Arizona courts denied appellate and post-conviction relief, Cook
filed a petition for writ of habeas corpus, which the district court denied and we
thereafter affirmed. Cook v. Schriro, 538 F.3d 1000 (9th Cir. 2008), cert. denied
129 S. Ct. 1033 (2009). On November 10, 2010, after the State sought a warrant of
execution, Cook filed this § 1983 action in which he raised several claims related
to the State’s use of sodium thiopental, one of three drugs used as part of execution
by lethal injection. The district court subsequently granted Defendants’ Rule
12(b)(6) motion to dismiss for failure to state a claim upon which relief may be
granted. Cook then timely filed this appeal.
We review de novo a district court’s order granting a motion to dismiss
under Rule 12(b)(6). Shroyer v. New Cingular Wireless Servs., Inc., 622 F.3d
1035, 1041 (9th Cir. 2010). A pleading must include a short and plain statement of
the claim showing that the pleader is entitled to relief. Fed. R. Civ. P. 8(a)(2).
“[T]he pleading standard Rule 8 announces does not require ‘detailed factual
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allegations,’ but it demands more than an unadorned,
the-defendant-unlawfully-harmed-me accusation.” Ashcroft v. Iqbal, 129 S. Ct.
1937, 1949 (2009) (quoting Bell Atl. Corp. v. Twombly, 550 U.S. 544, 555 (2007)).
“[A] plaintiff’s obligation to provide the grounds of his entitle[ment] to relief
requires more than labels and conclusions, and a formulaic recitation of the
elements of a cause of action will not do.” Twombly, 550 U.S. at 555 (internal
quotation marks omitted).
“A Rule 12(b)(6) motion tests the legal sufficiency of a claim. A claim may
be dismissed only if ‘it appears beyond doubt that the plaintiff can prove no set of
facts in support of his claim which would entitle him to relief.’” Navarro v. Block,
250 F.3d 729, 732 (9th Cir. 2001) (quoting Conley v. Gibson, 355 U.S. 41, 45–46
(1957)). “To survive a motion to dismiss, a complaint must contain sufficient
factual matter, accepted as true, to ‘state a claim to relief that is plausible on its
face.’” Iqbal, 129 S. Ct. at 1949 (quoting Twombly, 550 U.S. at 570). “A claim
has facial plausibility when the plaintiff pleads factual content that allows the court
to draw the reasonable inference that the defendant is liable for the misconduct
For a capital prisoner to establish an Eighth Amendment claim for exposure
to future harm of severe pain constituting cruel and unusual punishment from an
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Neither party disputes that the “sure or very likely” and “substantial
risk of serious harm” standard articulated by the plurality opinion in Baze is the
proper standard here. 553 U.S. at 50. Notably, in Dickens v. Brewer, 631 F.3d
1139 (9th Cir. 2011) we affirmed that, like every other circuit court to consider the
issue, “the Baze plurality’s substantial risk standard is the controlling standard for
assessing the constitutionality of an execution protocol.” Id. at 1144–46; citing
Brewer v. Landrigan, 131 S. Ct. 445 (2010) (holding that an Arizona execution
could proceed because there was no evidence that the drug was “‘sure or very
likely to cause serious illness and needless suffering’” (quoting Baze, 553 U.S. at
50) (emphasis omitted)); Raby v. Livingston, 600 F.3d 552, 557 (5th Cir. 2010);
Nooner v. Norris, 594 F.3d 592, 598–99 (8th Cir. 2010); Jackson v. Danberg, 594
F.3d 210, 219–22 (3d Cir. 2010); Cooey v. Strickland, 589 F.3d 210, 220 (6th Cir.
2009); Clemons v. Crawford, 585 F.3d 1119, 1125–26 (8th Cir. 2009); Harbison v.
Little, 571 F.3d 531, 535 (6th Cir. 2009); Emmett v. Johnson, 532 F.3d 291, 298
(4th Cir. 2008).
execution method, he is required to show that “the conditions presenting the risk
must be ‘sure or very likely to cause serious illness and needless suffering,’ and
give rise to ‘sufficiently imminent dangers.’” Baze v. Rees, 553 U.S. 35, 50 (2008)
(Roberts, C.J., plurality opinion) (quoting Helling v. McKinney, 509 U.S. 25, 33,
In Baze, the Court explained that “to prevail on such a claim there
must be a ‘substantial risk of serious harm,’ an ‘objectively intolerable risk of
harm’ that prevents prison officials from pleading that they were ‘subjectively
blameless for purposes of the Eighth Amendment.’” Id. (quoting Farmer v.
Brennan, 511 U.S. 825, 842, 846 & n.9 (1994)).
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Because Cook committed his crimes before November 23, 1992, he has the
choice to be executed by either lethal injection or lethal gas. See Ariz. Rev. Stat. §
13-757(B). Cook has not yet chosen a method of execution, and if he does not
make a choice, the ADC must use lethal injection to execute him. Id.
Arizona’s protocol for execution by lethal injection requires the sequential
administration of sodium thiopental, pancuronium bromide, and potassium
chloride. Dickens, 631 F.3d at 1142.
Sodium thiopental is a fast-acting barbiturate that anesthetizes the
inmate and permits the other chemicals to be administered without
causing pain. Pancuronium bromide is a paralytic neuromuscular
blocking agent that causes complete paralyzation and suffocation.
Potassium chloride induces cardiac arrest. It is uncontested on this
record that, if an inmate is not properly anesthetized by the sodium
thiopental at the start of the execution, he will experience significant
pain and suffering from the administration of the pancuronium
bromide and potassium chloride. If the sodium thiopental is
administered properly, however, there is no risk of pain during the
Underlying Cook’s claims is the fact that Arizona has obtained sodium
thiopental from a foreign source, rather than from the United States. In his reply
brief, Cook summarizes the five allegations raised in his Complaint, which he
asserts we must take as true. First, he alleges that the ADC “lacks the appropriate
safeguards to ensure the imported substance it obtained is not contaminated, is
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viable, and is actually sodium thiopental.” Second, “the substance was obtained in
violation of federal law.” Third, “a foreign-manufactured drug was produced in an
environment such that the drug may not be effective, and that the drug could be
contaminated or compromised.” Fourth, “drugs from foreign countries do not have
the same assurance of safety as drugs actually regulated by the FDA, due to the
risk that counterfeit or unapproved drugs will be sent to consumers and also
because without regulation of repackaging, storage conditions, and many other
factors, drugs delivered to the American public from foreign countries may be very
different from FDA approved drugs with respect to formulation, potency, quality,
and labeling” (quoting Iverson v. Pfizer, Inc. (In re Canadian Import Antitrust
Litig.), 470 F.3d 785, 789 (8th Cir. 2006) (internal citations omitted)). Fifth, “this
substance will cause Cook to suffer pain if the drug is contaminated, compromised,
or substandard, which in turn will cause excruciating pain when the next two drugs
Cook contends that the district court erred in granting Defendants’ motion to
dismiss for two reasons. First, he argues that the foreign manufactured non-FDA
approved sodium thiopental may be “contaminated, compromised, or otherwise
ineffective, such that it will not properly anesthetize him” or “might not actually be
sodium thiopental at all” and that “using an unapproved substance from an
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unknown manufacturer in an execution gives rise to a substantial risk of
unconstitutional pain” in violation of the Eighth Amendment. Second, Cook
contends that the administration of “an unapproved substance from an unknown
manufacturer in an execution by medical professionals constitutes deliberate
indifference” to his right to be free from cruel and unusual punishment in violation
of the Eighth Amendment.
At issue for both of these claims is whether Cook has sufficiently satisfied,
to survive a motion to dismiss, Rule 8(a)’s pleading requirements to state facially
plausible claims that the drug the ADC has obtained is “sure or very likely to cause
serious illness and needless suffering” in violation of his Eighth Amendment right
to be free from cruel and unusual punishment. See Baze, 553 U.S. at 50; see also
Iqbal, 129 S. Ct. at 1949 (pleading standard). We conclude that Cook’s allegations
fail to meet this standard.
While the pleading standard for Rule 8(a) is liberal, the “[f]actual allegations
must be enough to raise a right to relief above the speculative level.” Twombly,
550 U.S. at 555. In Iqbal, the Court noted that “[t]o survive a motion to dismiss, a
complaint must contain sufficient factual matter, accepted as true, to ‘state a claim
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to relief that is plausible on its face.’” Iqbal, 129 S. Ct. at 1949 (quoting Twombly,
550 U.S. at 570).
Cook’s allegations that foreign manufactured non-FDA approved drugs
“may not be effective,” “could be contaminated or compromised,” and “may be
very different from FDA approved drugs with respect to formulation, potency,
quality, and labeling” are all speculative and overly generalized claims applicable
to every drug produced outside the United States. Cook does not make any
specific allegations about the manufacturing process, formulation, potency, quality,
or labeling of the drug at issue here. Cook also fails to allege any facts to support
his claim that the drug might not actually be sodium thiopental or that it could be
contaminated, compromised, or otherwise substandard such that it may not
effectively anesthetize him and cause him unconstitutional pain when the next two
drugs are administered. Id. Cook’s allegation that the ADC lacks appropriate
safeguards to ensure the sodium thiopental it obtained “is not contaminated, is
viable, and is actually sodium thiopental” is also conclusory and without any
supporting factual allegations. Moreover, Cook’s assertion that “the substance was
obtained in violation of federal law” is again speculative and Cook has not made a
sufficient showing that the lack of FDA approval of the sodium thiopental at issue
here makes it sufficiently likely that the sodium thiopental is either not what it
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We express no view as to whether the sodium thiopental was obtained
in violation of federal law. The actual legality of importing this drug is not at issue
here, we are only concerned with the constitutionality of its use on Mr. Cook.
purports to be, or is otherwise adulterated.
Rather, Cook relies on his allegations
that Arizona’s sodium thiopental is imported and not approved by the FDA. But
Landrigan, 131 S. Ct. 445, advises that these facts are not sufficient to state a
plausible Eighth Amendment claim. Like the instant case, Landrigan involved an
Arizona death row inmate challenging Arizona’s use of imported,
non-FDA-approved sodium thiopental. Reversing the Ninth Circuit, the Supreme
Court held that the district court abused its discretion in granting Landrigan’s
motion for a preliminary injunction to stay his execution.
Cook distinguishes Landrigan on the grounds that it involved a preliminary
injunction, whereas the instant case involves a motion to dismiss. Thus, while
Landrigan had to provide enough evidence to make success on his claim “likely,”
Cook only needs to allege enough facts to make his claim “plausible.”
Nevertheless, the Court in Landrigan found “no evidence in the record to suggest
that the drug obtained from a foreign source is unsafe.” Id. This statement clearly
implies that the facts that Arizona’s sodium thiopental is imported and non-FDA
approved do not themselves constitute evidence of danger. Thus, in this case,
Cook’s bare allegations that the sodium thiopental is imported and non-FDA
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To the extent that Cook alleges that the process of administering a
substance that is not sodium thiopental, or is a diluted or adulterated version of
sodium thiopental could itself potentially cause him unconstitutional pain, he offers
no factual support to support such an assertion.
approved, even taken as true, do not plausibly suggest that the drug is “sure or very
likely to cause serious illness and needless suffering” or otherwise creates a
“substantial risk of serious harm” in violation of Cook’s Eighth Amendment right
to be free from cruel and unusual punishment sufficient to survive a motion to
dismiss. Baze, 553 U.S. at 50; see also Iqbal, 129 S. Ct. at 1949.
We also reject any claim Cook makes that the administration of the allegedly
incorrect, diluted or adulterated drug would cause him excrutiating pain when the
other two drugs are administered.
We have recently upheld Arizona’s lethal
injection protocol in Dickens, when we stated that “the protocol’s safeguards are
adequate under the Baze standard.” 631 F.3d at 1141. We noted the following
facts about the administration of the sodium thiopental:
After the sodium thiopental is administered, the [Members of
the Medical Team (“MTMs”)] confirm that the inmate is unconscious
by “sight and sound” using the camera and microphone, and an MTM
enters the execution chamber to physically confirm unconsciousness.
If the inmate is conscious, the Director of the [ADC] may order the
[Special Operations Team (“SOT”)] members to administer an
additional dose of sodium thiopental, and the MTMs go through the
same steps to verify unconsciousness. The SOT members cannot
administer the pancuronium bromide until the MTMs have confirmed
that the inmate is unconscious and at least three minutes have elapsed
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from the commencement of the administration of the sodium
thiopental. The IV lines are flushed with heparin/saline between each
injection, to ensure that they are clean and functioning properly.
Id. at 1143.
Nothing in Cook’s Complaint suggests that, even if he were to receive a
substance that was not sodium thiopental, or was diluted or adulterated and failed
to properly anesthetize him, Arizona’s protocol would fail to identify the problem
and halt the process to prevent the administration of the pancuronium bromide and
potassium chloride. Cook’s reliance on speculative and conclusory allegations is
insufficient to state a facially plausible claim that the sodium thiopental the ADC
has obtained is “sure or very likely to cause serious illness and needless suffering”
in violation of his Eighth Amendment right to be free from cruel and unusual
punishment. See Baze, 553 U.S. at 50; see also Iqbal, 129 S. Ct. at 1949. We
therefore affirm the district court as to Cook’s first claim.
Cook’s second claim is dependant on the sufficiency of his first claim. Cook
argues that the medical professionals who would administer the foreign-
manufactured non-FDA approved substance would know that administering this
drug involves substantial risks and that by administering the drug they would
demonstrate deliberate indifference to his medical needs. However, because Cook
fails to make a facially plausible claim that the sodium thiopental at issue here is
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“sure or very likely to cause serious illness and needless suffering,” or otherwise
creates a “substantial risk of serious harm” he cannot show that the medical
officials administering the drug would be medically indifferent. Id.
Because Cook has failed to demonstrate that the district court erred as to
either of his claims, the judgment of the district court is
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Jon M. Sands, Federal Public Defender, Dale A. Baich (argued), Robin C.
Konrad, Golnoosh Farzaneh, Assistant Federal Public Defenders, Phoenix,
Arizona, for the plaintiff-appellant.
Thomas C. Horne, Attorney General, Kent E. Cattani (argued), Chief
Counsel, Capital Litigation Section, Phoenix, Arizona, for the defendant-appellee.
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