US Dep't of Justice v. Ricco Jonas

24 F.4th 718
Court of Appeals for the First Circuit·Decided January 27, 2022·No. 19-1243P·Published·Cited by 1 cases

Opinion

United States Court of Appeals For the First Circuit

No. 19-1243 UNITED STATES DEPARTMENT OF JUSTICE, Petitioner, Appellee,

v.

MICHELLE RICCO JONAS,

Respondent, Appellant.

APPEAL FROM THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF NEW HAMPSHIRE

[Hon. Landya B. McCafferty, U.S. District Judge]

Before

Howard, Chief Judge,

and Thompson,* Circuit Judge.

Anthony J. Galdieri, Senior Assistant Attorney General, with whom Gordon J. MacDonald, Attorney General, and Lawrence M. Edelman, Assistant Attorney General, were on brief, for Appellant.

Seth R. Aframe, Assistant United States Attorney, with whom Scott W. Murray, United States Attorney, was on brief, for Appellee.

Nathan Freed Wessler, with whom Brett Max Kaufman and Jennifer Stisa Granick were on brief, for American Civil Liberties Union Foundation, amicus curiae.

Gilles R. Bissonnette and Henry Klementowicz, on brief

* Judge Torruella heard oral argument in this matter and participated in the semble, but he did not participate in the issuance of the panel's opinion. The remaining two panelists therefore issued the opinion pursuant to 28 U.S.C. § 46(d).

for ACLU of New Hampshire Foundation, amicus curiae.

Zachary L. Heiden and Emma E. Bond, on brief for American Civil Liberties Union of Maine, amicus curiae.

Matthew R. Segal and Jessie J. Rossman, on brief for American Civil Liberties Union Foundation of Massachusetts, Inc., amicus curiae.

William Ramírez, on brief for American Civil Liberties Union of Puerto Rico, amicus curiae.

Robert B. Mann and Robert B. Mann Law Office, on brief for ACLU of Rhode Island, amicus curiae.

January 27, 2022

HOWARD, Chief Judge. Respondent-appellant Michelle Ricco Jonas ("Ricco Jonas"), the Program Manager for New Hampshire's Prescription Drug Monitoring Program (the "PDMP"), appeals from a district court judgment ordering compliance with an administrative subpoena issued to her by the United States Drug Enforcement Administration ("DEA") pursuant to 21 U.S.C. § 876, to produce the PDMP-kept prescription drug records of an individual.1 On appeal, Ricco Jonas contends that the subpoena is unenforceable because, although it was issued to her and 21 U.S.C. § 876(c) authorizes the enforcement of a "subp[o]ena issued to any person," in her view, the subpoena really targeted the State of New Hampshire and states are not "person[s]" within the meaning of 21 U.S.C. § 876(c) against whom administrative subpoenas may be issued and enforced. Additionally, she argues that, even if 21 U.S.C. § 876(c) generally authorizes the enforcement of administrative subpoenas against a state, the Fourth Amendment still poses a bar to compliance because the subpoena-specified individual has a reasonable expectation of privacy in his prescription drug records, thereby allowing disclosure only after a finding of probable cause by a court. After careful

1During the pendency of this appeal, Ricco Jonas informed us that she is no longer the PDMP program manager. Nevertheless, neither party has suggested that the appeal is moot.

consideration, we reject both of Ricco Jonas's contentions and affirm the district court judgment.

I. STATUTORY BACKGROUND

A. The Controlled Substances Act In 1970, Congress enacted the Comprehensive Drug Abuse Prevention and Control Act (the "Act"), Pub. L. No. 91-513, 84 Stat. 1236, to "consolidate various drug laws on the books into a comprehensive statute, provide meaningful regulation over legitimate sources of drugs to prevent diversion into illegal channels, and strengthen law enforcement tools against the traffic in illicit drugs." Gonzales v. Raich, 545 U.S. 1, 10 (2005). The main objectives of Title II of the Act, the Controlled Substances Act ("CSA"), 21 U.S.C. § 801 et seq., are "to conquer drug abuse and to control the legitimate and illegitimate traffic in controlled substances."2 Raich, 545 U.S. at 12; id. at 12-13 ("Congress was particularly concerned with the need to prevent the diversion of drugs from legitimate to illicit channels."). To achieve these goals, Congress established a "closed regulatory

2 The CSA categorizes controlled substances into five schedules (I through V), based on the drugs' potential for abuse, accepted medical uses, and likelihood of causing psychological or physical dependency. 21 U.S.C. § 812. Drugs categorized in schedules II through V have "a currently accepted medical use in treatment in the United States" or "a currently accepted medical use with severe restrictions." Id. §§ 812(b)(2)-(5). Schedule I drugs do not have any accepted medical use. Id. § 812(b)(1).

system" that makes it unlawful "to manufacture, distribute, dispense, or possess any controlled substance except as authorized by the CSA." Id. at 13 (citing 21 U.S.C. §§ 841(a)(1), 844(a)). As part of this regulatory system, "[t]he CSA requires manufacturers, physicians, pharmacies, and other handlers of controlled substances to comply with statutory and regulatory provisions mandating registration with the DEA, compliance with specific production quotas, security controls to guard against diversion, recordkeeping and reporting obligations, and prescription requirements." Id. at 27 (citing 21 U.S.C. §§ 821- 830; 21 C.F.R. § 1301 et seq. (2004)).

The CSA authorizes the Attorney General to issue administrative subpoenas to investigate suspected illicit drug activity. See 21 U.S.C. § 876. Specifically, § 876(a) of the statute provides in relevant part that,

In any investigation . . . with respect to controlled substances . . . the Attorney General may subpe[o]na witnesses, compel the attendance and testimony of witnesses, and require the production of any records (including books, papers, documents, and other tangible things which constitute or contain evidence) which the Attorney General finds relevant or material to the investigation. The attendance of witnesses and the production of records may be required from any place in any State or in any territory or other place subject to the jurisdiction of the United States . . . .

Id. § 876(a). The Attorney General has delegated this authority to the DEA. See id. § 878(a)(2); 28 C.F.R. §§ 0.100, 0.104, Appendix to Subpart R, Section 4.

Section 876(c) of the CSA provides for judicial enforcement of subpoenas issued under § 876(a). It states that,

In the case of contumacy by or refusal to obey a subp[o]ena issued to any person, the Attorney General may invoke the aid of any court of the United States within the jurisdiction of which the investigation is carried on or of which the subp[o]enaed person is an inhabitant, or in which he carries on business or may be found, to compel compliance with the subp[o]ena. The court may issue an order requiring the subp[o]enaed person to appear before the Attorney General to produce records, if so ordered, or to give testimony touching the matter under investigation. Any failure to obey the order of the court may be punished by the court as a contempt thereof. All process in any such case may be served in any judicial district in which such person may be found.

21 U.S.C. § 876(c). The CSA provides that state law is preempted whenever "there is a positive conflict between [a] provision of th[e] [CSA] and [a] State law so that the two cannot consistently stand together." Id. § 903. B. The PDMP and New Hampshire Law In 2012, the New Hampshire legislature established the PDMP to "enhanc[e] patient care, curtail[] the misuse and abuse of controlled substances, combat[] illegal trade in and diversion of controlled substances, and enabl[e] access to prescription information by practitioners, dispensers, and other authorized individuals and agencies."3 New Hampshire PDMP, https://www.newhampshirepdmp.com/ (last visited Jan. 27, 2022).

3 The PDMP is currently administered by the New Hampshire Department of Health and Human Services. N.H. Rev. Stat. Ann.

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