United States v. Gas PipeUnited States v. Gas Pipe
Plaintiff-Appellee,
versus
GAS PIPE, INCORPORATED; AMY LYNN, INCORPORATED; GERALD SHULTS; AMY HERRIG,
Defendants-Appellants.
Before HAYNES, HIGGINSON, and OLDHAM, Circuit Judges.
Appellants Gerald Shults and Amy Herrig, along with two corporate entities that they owned and controlled, owned and operated a chain of smoke shops in Texas and New Mexico. The stores sold synthetic cannabinoids branded as “herbal incense,” “potpourri,” or “aroma therapy products.” These products, commonly known as “spice,” were labeled “not for human consumption” even though the appellants intended them for exactly that. In late 2013, the Drug Enforcement Administration initiated an undercover investigation into the appellants’ spice sales, eventually resulting in their arrest and prosecution. After a three-week trial, a jury convicted the appellants of one count of conspiracy to defraud the United States, based on their efforts to defraud the Food and Drug Administration and to misbrand drugs.
On appeal, the appellants argue that the district court erred by failing to strike the fraud theory of the indictment, by incorrectly instructing the jury, and by denying their motion for acquittal due to insufficient
I.
Appellants Gas Pipe, Inc., Amy Lynn, Inc., Gerald Shults, and Amy Herrig owned and operated a chain of smoke shops in Texas and New Mexico.1 Among the products on offer at Gas Pipe stores were synthetic-cannabinoid products branded as “herbal incense,” “potpourri,” or “aroma therapy products,” commonly known as “spice.” Spice, when smoked, produces a stimulant, depressant, or hallucinogenic effect on the central nervous system.
For the past decade, the federal government has scheduled various synthetic cannabinoids as illegal controlled substances. Given that there are more than 700 known synthetic cannabinoids, the process of scheduling is iterative, with more synthetic cannabinoids being scheduled as the Drug Enforcement Agency (“DEA“) and Food and Drug Administration (“FDA“) analyze them and their effects. But regardless of whether a synthetic cannabinoid has been scheduled, it may not be sold for human consumption absent FDA approval and proper labeling.
The appellants labeled their products as “not for human consumption.” But, as the appellants stipulated at trial, they knew that the spice products sold by Gas Pipe stores were mislabeled because they were intended for human consumption. Indeed, Gas Pipe‘s spice products were sometimes rated based on their “strength,” meaning how “high” it would get the user. Between 2011 and 2014, the appellants sold more than two million units of spice totaling more than $40 million in revenue.
In late 2013, the DEA started an undercover investigation into the appellants’ spice sales. DEA agents posed as customers and made 34 “controlled buys” to determine whether the appellants were selling spice for human consumption. The agents had the spice analyzed by a lab, and results revealed that the spice contained various synthetic cannabinoids. On June 4, 2014, DEA agents executed search warrants at all of the appellants’ stores and warehouses and seized spice containing synthetic cannabinoids, some of which had already been scheduled as controlled substances.
A grand jury returned a Third Superseding Indictment in September 2016. The indictment charged the appellants and six of their employees with 11 counts.2 Count One charged the appellants with violating
misbranded drug into interstate commerce with the intent to defraud or mislead.”
After a three-week trial, the jury found the appellants guilty on Count One and acquitted them on the remaining counts.3
II.
The appellants first make two arguments as to why Count One of the indictment was legally insufficient. Because they preserved their challenges, we review them de novo. United States v. Anderton, 901 F.3d 278, 282 (5th Cir. 2018).
First, the appellants argue that the word “defraud,” as used in
Second, the appellants argue that this court should impose a “limiting principle” on
These same two legal arguments also form the basis of the appellants’ challenge to the district court‘s conspiracy-to-defraud jury instructions, and thus that challenge also fails. The appellants preserved their objections to the conspiracy-to-defraud instructions. We ordinarily review jury instructions for abuse of discretion. But when, as here, the appellants argue that the instruction misstates an element of the offense, that is an issue of statutory construction, which we review de novo subject to harmless error review. United States v. Garcia-Gonzalez, 714 F.3d 306, 312 (5th Cir. 2013); United States v. Guevara, 408 F.3d 252, 257 (5th Cir. 2005).
Specifically, the appellants argue that the district court committed reversible error in its conspiracy-to-defraud jury instructions by (1) failing to limit the defraud theory to agreements to cheat the Government out of money or property and (2) refusing to provide a Marinello instruction that the Government must prove a nexus between the conspiracy and a particular administrative proceeding. Because we rejected the appellants’ two legal arguments above about the scope of
III.
The appellants next challenge the district court‘s jury instructions about felony misbranding in two respects. First, they argue that
A.
The appellants’ first claim of instructional error—that the district court failed to include materiality as an element of felony misbranding—asserts misstatement of an element and hinges on statutory interpretation. The court‘s review is therefore de novo, subject to harmless error analysis. See Garcia-Gonzalez, 714 F.3d at 312; Guevara, 408 F.3d at 257.
Section 333 of the Food, Drug, and Cosmetic Act (“FDCA“) imposes felony liability for misbranding drugs with the “intent to defraud or mislead.”
In Neder, the Supreme Court considered whether materiality is an element of a “scheme or artifice to defraud” under the federal mail fraud (
Assuming without deciding that materiality is an element of
To the extent that the district court erred in omitting materiality as an element of
Our review of the record shows, beyond a reasonable doubt, that the jury would have concluded that the appellants’ misbranding tended to influence, or was capable of influencing, the FDA‘s decisionmaking based on evidence presented at trial.
First, Lawrence Shahwan, who supplied spice to the appellants, testified that the reason he labeled his product “Not for Human Consumption” was because that was “the only way that we could sell it to the public. If it was stated for human consumption, it would be subject to FDA
Although the Government highlights other evidence—including emails and contemporaneous notes that show the appellants were monitoring FDA actions regarding spice and additional witness testimony about the appellants’ knowledge of the regulatory landscape—Shahwan‘s and Campbell‘s testimony are sufficient to show that the appellants sold spice labeled “Not for Human Consumption” to evade the FDA‘s regulatory scrutiny and that, if the appellants’ products had been correctly labeled as intended for human consumption, they would have been subject to FDA regulation. The mislabeling therefore had “a natural tendency to influence, or [was] capable of influencing” the FDA‘s decisionmaking and thus was “material.” Neder, 527 U.S. at 16.
B.
The appellants’ second claim is that the district court should have specifically defined
This argument presents a “framing” issue reviewed for abuse of discretion. Eastman Chem. Co. v. Plastipure, Inc., 775 F.3d 230, 240 (5th Cir. 2014); see also United States v. Jones, 664 F.3d 966, 978 (5th Cir. 2011). Under that standard, “[w]e will reverse the district court‘s decision only if the requested instruction (1) was a substantially correct statement of the law, (2) was not substantially covered in the charge as a whole, and (3) concerned an important point in the trial such that the failure to instruct the jury on the issue seriously impaired the defendant‘s ability to present a given defense.” United States v. Wright, 634 F.3d 770, 775 (5th Cir. 2011) (internal quotation marks omitted) (quoting Cooper Indus., Inc. v. Tarmac Roofing Sys., Inc., 276 F.3d 704, 714 (5th Cir. 2002)). We “afford the trial court great latitude in the framing and structure of jury instructions.” Eastman, 775 F.3d at 240.
Count One of the indictment charged the appellants with conspiring to defraud the United States by (1) conspiring to defraud the FDA and (2) conspiring to introduce misbranded drugs into interstate commerce with the intent to defraud or mislead. When instructing the jury about the conspiracy to defraud the FDA, the district court separately defined “defraud“: “The word ‘defraud’ here is not limited to its ordinary meaning of cheating the government out of money or property; it also includes impairing, obstructing, defeating, or interfering with the lawful function of the government or one if its agencies by dishonest means.” When instructing the jury about conspiracy to commit felony misbranding, the district court did not separately define “defraud,” but when instructing the jury about the lesser included offense, conspiracy to commit simple
This court rejected a similar argument in United States v. Haas, 171 F.3d 259 (5th Cir. 1999). Like the appellants, the defendant in that case was convicted of conspiracy to defraud the FDA and conspiracy to commit felony misbranding. Id. at 263-64. Also like the appellants, the defendant argued that “the district court erred when it failed to define the phrase ‘intent to defraud’ under
The appellants try to distinguish Haas by pointing out that the jury instructions in that case did at least specify that fraudulent misbranding requires “deceit, craft or trickery or at least . . . means that are dishonest.” Here, however, the district court‘s instructions on the meaning of “defraud” included a similar gloss, referencing “cheating” and “dishonest means.” The appellants do not explain why these words should be deemed inadequate. Moreover, courts have interpreted
The appellants also argue that the district court erred by not instructing the jury that an “intent to deceive or cheat” must be “connected” to misbranding. We disagree. Although the district court did not adopt the exact wording proposed by the appellants, it instructed the jury that a conviction for felony misbranding required a finding “[t]hat a person mislabeled the drug and the defendant, by such mislabeling, intended to defraud or mislead.”
For these reasons, the district court‘s jury instruction “substantially covered” the appellants’ proposed instruction and did not misstate the law. Wright, 634 F.3d at 775.
IV.
The appellants next challenge the sufficiency of the evidence for conviction under Count One.
The parties agree that the appellants preserved their sufficiency challenges to their convictions by timely moving for acquittal under
A.
The appellants raise a combination of legal and factual challenges to the sufficiency of the evidence supporting their convictions for conspiracy to defraud the FDA. They assert that (1) Marinello upsets their conviction because there was insufficient evidence showing that the appellants agreed to interfere with or obstruct “a particular administrative proceeding“; (2) the FDA could not have been defrauded because there was no evidence of an ongoing FDA investigation into their spice sales before the June 2014 raid; and (3) the evidence was insufficient for the jury to rationally conclude that they intended to defraud the FDA.
First, the appellants reprise their argument that Marinello, 138 S. Ct. 1101, required the Government to put on evidence that they agreed to interfere with or obstruct a particular FDA proceeding that was then pending or reasonably foreseeable. For the reasons already discussed, supra section II, the Government was not required to make this showing.
Second, the appellants claim that the FDA could not have been defrauded within the meaning of
Third, the appellants assert that the Government did not present evidence from which the jury could conclude that they intended to defraud the FDA. We disagree. As discussed, supra section III.A, the appellants’ supplier, Lawrence Shahwan, and their employee, Joshua Campbell, both testified that the appellants labeled these products “not for human consumption” to avoid scrutiny or regulation by the FDA. Shahwan also testified that it was obvious that the products could not have been sold if intended for human consumption. Viewing the evidence in the light most favorable to the Government and all reasonable inferences in support of the jury‘s verdict, Bolton, 908 F.3d at 89, we conclude that a rational jury could find that the evidence was sufficient
B.
The appellants also argue that the evidence was insufficient to prove the felony misbranding offense because the Government did not establish beyond a reasonable doubt that the public was misled by the labeling or that the appellants intended to defraud or mislead the Government. We need not reach this question. The district court gave a unanimity instruction, and the jury convicted the appellants on Count One after separately concluding that the appellants conspired to defraud the FDA and also that they conspired to commit felony misbranding. The appellants’ convictions on Count One can be sustained by our conclusion that the evidence was sufficient to convict the appellants of conspiring to defraud the FDA. See United States v. Mauskar, 557 F.3d 219, 229 (5th Cir. 2009) (“[A] general guilty verdict on a multiple-object conspiracy may stand even if the evidence is insufficient to sustain a conviction on one of the charged objects.” (alteration in original) (quoting United States v. Mann, 493 F.3d 484, 492 (5th Cir. 2007))).
V.
Finally, Shults and Herrig appeal the substantive reasonableness of their 36-month sentences, which we review for abuse of discretion. United States v. Sifuentes, 945 F.3d 865, 868 (5th Cir. 2019).
“This court recognizes three types of sentences: (1) a sentence within a properly calculated Guidelines range; (2) a sentence that includes an upward or downward departure as allowed by the Guidelines; and (3) a non-Guideline sentence or a variance that is outside of the relevant Guidelines range.” United States v. Brantley, 537 F.3d 347, 349 (5th Cir. 2008) (internal quotation marks omitted) (quoting United States v. Smith, 440 F.3d 704, 706-08 (5th Cir. 2006)). If “the district court imposes a sentence that is outside the guidelines framework, such a sentence is considered a variance.” United States v. Jacobs, 635 F.3d 778, 782 (5th Cir. 2011) (internal quotation marks omitted). The district court must explain its reasons for imposing any variance under the
Contrary to Shults and Herrig‘s assertion, the district court imposed their sentences as upward variances after carefully considering the
In their opening brief, Shults and Herrig incorrectly argue that the variance rested “on the same ground” as the departure,
Because the district court justified Shults‘s and Herrig‘s sentences as both variances and departures, we need not consider the propriety of their sentences as an upward departure. Instead, we affirm the sentences on the district court‘s basis as an upward variance justified by the
VI.
We AFFIRM the district court on all issues, holding that the allegations in Count One of the indictment charging the appellants with conspiracy to defraud the FDA in violation of