[Congressional Record Volume 172, Number 145 (Tuesday, September 15, 2026)]
[House]
[Pages H5674-H5676]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]




                        STOP PILLS THAT KILL ACT

  Mr. GUTHRIE. Mr. Speaker, I move to suspend the rules and pass the 
bill (H.R. 8005) to amend the Controlled Substances Act to prohibit 
certain acts related to fentanyl, analogues of fentanyl, and 
counterfeit substances, and for other purposes, as amended.
  The Clerk read the title of the bill.
  The text of the bill is as follows:

                               H.R. 8005

       Be it enacted by the Senate and House of Representatives of 
     the United States of America in Congress assembled,

     SECTION 1. SHORT TITLE.

       This Act may be cited as the ``Stop Pills That Kill Act''.

     SEC. 2. REGULATION OF CERTAIN MACHINES.

       (a) Definitions.--Section 102 of the Controlled Substances 
     Act (21 U.S.C. 802) is amended--
       (1) by striking paragraph (38) and inserting the following:
       ``(38) The term `regulated person' means a person who--
       ``(A) manufactures, distributes, imports, or exports a 
     listed chemical;
       ``(B) manufactures, distributes, delivers, sells, imports, 
     or exports a tableting machine, encapsulating machine, or 
     critical part of a tableting or encapsulating machine; or
       ``(C) acts as a broker or trader for a regulated 
     transaction involving a listed chemical, tableting machine, 
     encapsulating machine, or critical part of a tableting or 
     encapsulating machine.'';
       (2) by striking paragraph (39)(B) and inserting the 
     following:
       ``(B) a distribution, delivery, sale, importation, 
     exportation, or international transaction of a tableting 
     machine, encapsulating machine, or critical part of a 
     tableting or encapsulating machine.'';
       (3) in paragraph (42), by inserting ``, tableting machine, 
     encapsulating machine, or critical part of a tableting or 
     encapsulating machine'' after ``listed chemical'';
       (4) in paragraph (43), in the matter preceding subparagraph 
     (A)--
       (A) by striking ``an international'' and inserting ``a 
     regulated''; and
       (B) by inserting ``, tableting machine, encapsulating 
     machine, or critical part of a tableting or encapsulating 
     machine'' after ``listed chemical''; and
       (5) by adding at the end the following:
       ``(61) The term `critical part', when used in reference to 
     a tableting or encapsulating machine, means any of the 
     following integral parts of a tableting or encapsulating 
     machine:
       ``(A) An upper punch.
       ``(B) A lower punch.
       ``(C) A die.
       ``(D) Any additional parts that the Attorney General has 
     determined to be integral to the operation of a tableting or 
     encapsulating machine, provided that such determination--
       ``(i) is made through rulemaking; and
       ``(ii) does not go into effect until the rulemaking process 
     has been completed.
       ``(62) The term `die' means a tool that serves as the mold 
     in which a product is compressed to form the desired size and 
     shape of a tablet or capsule.
       ``(63) The term `lower punch' means the punch inserted into 
     the turret below the die.
       ``(64) The term `punch' means a rod-shaped tool used in 
     producing tablets and other products.
       ``(65) The term `upper punch' means the punch inserted into 
     the turret above the die.''.
       (b) Regulation.--
       (1) Records of regulated transactions.--Section 310(a) of 
     the Controlled Substances Act (21 U.S.C. 830(a)) is amended--
       (A) in paragraph (1), by striking ``or an encapsulating 
     machine'' and inserting ``, encapsulating machine, or 
     critical part of a tableting or encapsulating machine''; and
       (B) in paragraph (2)--
       (i) by striking ``or encapsulating machine'' and inserting 
     ``, encapsulating machine, or critical part of a tableting or 
     encapsulating machine''; and
       (ii) by inserting before the period at the end the 
     following: ``and shall identify the tableting machine, 
     encapsulating machine, or critical part of a tableting or 
     encapsulating machine by means of a serial number that is 
     engraved, cast, or otherwise permanently affixed to a 
     nonremovable part of the tableting machine, encapsulating 
     machine, or critical part of a tableting or encapsulating 
     machine''.
       (2) Reports to attorney general.--Section 310(b)(1) of the 
     Controlled Substances Act (21 U.S.C. 830(b)(1)) is amended by 
     striking subparagraph (D) and inserting the following:
       ``(D) any regulated transaction in a tableting machine, 
     encapsulating machine, or critical part of a tableting or 
     encapsulating machine, including the serial number affixed to 
     the tableting machine, encapsulating machine, or critical 
     part of a tableting or encapsulating machine.''.
       (3) Regulations.--
       (A) In general.--Not later than 180 days after the date of 
     enactment of this Act, the Attorney General shall promulgate 
     regulations carrying out the amendments made by paragraphs 
     (1) and (2).
       (B) Inclusion.--The regulations required under subparagraph 
     (A) shall include requirements regarding serial numbers 
     affixed to tableting machines, encapsulating machines, or 
     critical parts of tableting or encapsulating machines 
     manufactured on or before the date of enactment of this Act.
       (4) Applicability.--
       (A) In general.--Except as specified in subparagraph (B), 
     the amendments made by paragraphs (1) and (2) shall apply 
     only to any tableting machine, encapsulating machine, or

[[Page H5675]]

     critical part of a tableting or encapsulating machine 
     manufactured, distributed, delivered, sold, imported, 
     exported, or included in an international transaction after 
     the effective date of the regulations promulgated under 
     paragraph (3).
       (B) Exception.--Beginning on the date that is 180 days 
     after the date of the enactment of this Act, the amendments 
     made by paragraph (1) of this subsection to paragraphs (1) 
     and (2) of section 310(a) of the Controlled Substances Act 
     (21 U.S.C. 830(a)) shall apply with respect to a tableting 
     machine, encapsulating machine, or critical part of a 
     tableting or encapsulating machine manufactured on or before 
     the date of enactment of this Act.
       (c) Prohibited Acts.--Section 403(a) of the Controlled 
     Substances Act (21 U.S.C. 843(a)) is amended--
       (1) in paragraph (8), by striking ``or'' at the end;
       (2) in paragraph (9), by striking the period at the end and 
     inserting a semicolon; and
       (3) by adding at the end the following:
       ``(10) to remove, alter, or obliterate any serial number 
     affixed to a tableting machine, encapsulating machine, or 
     critical part of a tableting or encapsulating machine, that 
     is required to have a serial number and with reasonable cause 
     to believe the serial number is so required; or
       ``(11) to transport, ship, receive, possess, distribute, 
     deliver, sell, import, or export a tableting machine, 
     encapsulating machine, or critical part of a tableting or 
     encapsulating machine that is required to have a serial 
     number, knowing that the serial number has been removed, 
     altered, or obliterated, and with reasonable cause to believe 
     the serial number is so required.''.

     SEC. 3. PROVIDING FOR EXTRATERRITORIAL JURISDICTION.

       (a) Possession, Manufacture, or Distribution for Purposes 
     of Unlawful Importation.--Section 1009 of the Controlled 
     Substances Act (21 U.S.C. 959) is amended--
       (1) by redesignating subsections (c) and (d) as subsections 
     (d) and (e), respectively;
       (2) by inserting after subsection (b) the following:
       ``(c) It shall be unlawful for any person to manufacture or 
     distribute a tableting machine, encapsulating machine, or 
     critical part of a tableting or encapsulating machine--
       ``(1) intending or knowing that the tableting machine, 
     encapsulating machine, or critical part of a tableting or 
     encapsulating machine will be used to illicitly manufacture a 
     controlled substance or listed chemical; and
       ``(2) intending, knowing, or having reasonable cause to 
     believe that the tableting machine, encapsulating machine, or 
     critical part of a tableting or encapsulating machine will be 
     unlawfully imported into the United States.''; and
       (3) in subsection (d), as so redesignated--
       (A) in paragraph (1), by striking ``or'' at the end;
       (B) in paragraph (2), by striking the period at the end and 
     inserting ``; or''; and
       (C) by adding at the end the following:
       ``(3) manufacture or distribute a tableting machine, 
     encapsulating machine, or critical part of a tableting or 
     encapsulating machine--
       ``(A) intending or knowing that the tableting machine, 
     encapsulating machine, or critical part of a tableting or 
     encapsulating machine will be used to illicitly manufacture a 
     controlled substance or listed chemical; and
       ``(B) intending, knowing, or having reasonable cause to 
     believe that the tableting machine, encapsulating machine, or 
     critical part of a tableting or encapsulating machine will be 
     unlawfully imported into the United States.''.
       (b) Prohibited Acts.--Section 1010 of the Controlled 
     Substances Act (21 U.S.C. 960) is amended--
       (1) in subsection (d)--
       (A) in paragraph (6), by striking ``or'' at the end;
       (B) in paragraph (7)--
       (i) by striking ``section 959 of this title'' and inserting 
     ``section 1009''; and
       (ii) by striking the period at the end and inserting ``; 
     or'';
       (C) by inserting after paragraph (7) the following:
       ``(8) manufactures or distributes a tableting machine, 
     encapsulating machine, or critical part of a tableting or 
     encapsulating machine in violation of section 1009,''; and
       (D) in the matter following paragraph (8), as so inserted, 
     by striking ``shall be fined'' and all that follows through 
     ``or both'' and inserting the following: ``shall be fined in 
     accordance with title 18, United States Code, imprisoned for 
     the applicable period described in subsection (e), or both''; 
     and
       (2) by adding at the end the following:
       ``(e) The applicable period described in this subsection is 
     the following:
       ``(1) In the case of a violation of paragraph (1) or (3) of 
     subsection (d) involving a list I chemical, not more than 20 
     years.
       ``(2) Subject to paragraph (4), in the case of a violation 
     of paragraph (7) of subsection (d), not more than 10 years.
       ``(3) Subject to paragraph (4), in the case of a violation 
     of paragraph (8) of subsection (d), not more than 8 years.
       ``(4) In the case of a violation of paragraph (7) or (8) of 
     subsection (d) that involves more than 1,000 kilograms of a 
     chemical or product or more than 100 machines that are 
     tableting machines or encapsulating machines, not more than 
     15 years.
       ``(5) In the case of any other violation of subsection (d), 
     not more than 10 years.''.
       (c) United States Sentencing Commission.--Pursuant to its 
     authority under section 994(p) of title 28, United States 
     Code, the United States Sentencing Commission shall review 
     and amend the Federal sentencing guidelines and policy 
     statements of the Commission in accordance with this Act and 
     the amendments made by this Act.

     SEC. 4. COUNTERFEIT PILLS CONTAINING AN ILLICIT SYNTHETIC 
                   SUBSTANCE.

       (a) Definition.--In this Act, the term ``counterfeit pill 
     containing an illicit synthetic substance'' means a substance 
     in pill or tablet form that--
       (1) is a counterfeit substance, as defined in section 
     102(7) of the Controlled Substances Act (21 U.S.C. 802(7)); 
     and
       (2) contains fentanyl, an analogue of fentanyl, a fentanyl-
     related substance, methamphetamine, an illicit depressant or 
     stimulant substance, an illicit narcotic, or an illicit 
     synthetic opioid.
       (b) Prohibited Acts.--Section 403(d)(2) of the Controlled 
     Substances Act (21 U.S.C. 843(d)(2)) is amended, in the 
     matter preceding subparagraph (A), by inserting ``, fentanyl, 
     an analogue of fentanyl, or a fentanyl-related substance'' 
     after ``methamphetamine''.
       (c) Comprehensive Plan.--
       (1) In general.--Not later than 180 days after the date of 
     enactment of this Act, the Administrator of the Drug 
     Enforcement Administration shall establish and implement an 
     operation and response plan to address counterfeit pills 
     containing an illicit synthetic substance.
       (2) Contents.--The plan required under paragraph (1) shall 
     include--
       (A) strategies to enable and empower Federal law 
     enforcement efforts to investigate and seize counterfeit 
     pills containing an illicit synthetic substance;
       (B) specific ways that education and prevention efforts to 
     stop the use of counterfeit pills containing an illicit 
     synthetic substance will be increased, including--
       (i) how ongoing efforts, such as Operation Engage, are 
     effective in increasing education and prevention; and
       (ii) how such ongoing efforts are tailored to youth and 
     teen access; and
       (C) an audit of current campaigns on counterfeit pills 
     containing an illicit synthetic substance, including a review 
     of data and other available information on how the campaigns 
     can be tailored, adjusted, or improved to better address the 
     flow of such counterfeit pills.
       (3) Report to congress.--
       (A) Report.--Not later than 1 year after the date of 
     enactment of this Act, and every year thereafter through 
     fiscal year 2031, the Attorney General, in consultation with 
     the Administrator of the Drug Enforcement Administration and 
     the Director of the Office of National Drug Control Policy, 
     shall submit to Congress a report containing information 
     regarding the collection of counterfeit pills containing an 
     illicit synthetic substance and prosecutions undertaken in 
     connection with such counterfeit pills.
       (B) Contents.--The report required under subparagraph (A) 
     shall include the following:
       (i) Data on the aggregate number of counterfeit pills 
     containing an illicit synthetic substance that have been 
     seized and collected by Federal law enforcement agencies.
       (ii) A description of pharmaceutical markings used for 
     counterfeit pills containing an illicit synthetic substance, 
     including how the markings compare to required labeling for 
     products approved by the Food and Drug Administration.
       (iii) A breakdown of which illicit substances are present 
     in counterfeit pills containing an illicit synthetic 
     substance.
       (iv) Data outlining the geographic origin and points of 
     seizure of counterfeit pills containing an illicit synthetic 
     substance.
       (v) Data on the charges filed pursuant to paragraph (1) or 
     (2) of section 401(a) of the Controlled Substances Act (21 
     U.S.C. 841(a)) in relation to counterfeit pills containing an 
     illicit synthetic substance, unless disclosure of the data 
     would--

       (I) require unsealing an indictment; or
       (II) undermine investigations and charges brought by the 
     Department of Justice.

       (vi) Data on the convictions and sentences against those 
     who are found guilty under paragraph (1) or (2) of section 
     401(a) of the Controlled Substances Act (21 U.S.C. 841(a)) as 
     it pertains to counterfeit pills containing an illicit 
     synthetic substance.
       (vii) Any prevention measures that the Department of 
     Justice, the Drug Enforcement Administration, or the Office 
     of National Drug Control Policy are undertaking to limit and 
     reduce the spread of counterfeit pills containing an illicit 
     synthetic substance, including ongoing public awareness 
     campaigns.

  The SPEAKER pro tempore. Pursuant to the rule, the gentleman from 
Kentucky (Mr. Guthrie) and the gentlewoman from Texas (Mrs. Fletcher) 
each will control 20 minutes.
  The Chair recognizes the gentleman from Kentucky.


                             General Leave

  Mr. GUTHRIE. Mr. Speaker, I ask unanimous consent that all Members 
may have 5 legislative days to revise and extend their remarks on the 
legislation and include extraneous material on H.R. 8005.
  The SPEAKER pro tempore. Is there objection to the request of the 
gentleman from Kentucky?
  There was no objection.
  Mr. GUTHRIE. Mr. Speaker, I yield myself such time as I may consume.
  Mr. Speaker, I rise today in strong support of H.R. 8005, the Stop 
Pills That Kill Act, that my good friend from Colorado (Mr. Evans) has 
brought forward.

[[Page H5676]]

  The threat posed by illicit pill presses has risen as drug 
traffickers continue to press fentanyl, methamphetamine, and other 
illicit drugs into drug pills.
  In 2025 alone, DEA seized over 47 million fentanyl-laced counterfeit 
pills. This bill makes important regulatory changes to strengthen DEA's 
ability to stop bad actors from misusing pill presses, tableting, and 
encapsulating machines and their critical components to illicitly 
manufacture controlled substances to poison our communities.
  This bill will make our streets safer.
  I applaud the tireless efforts of my friend from Colorado to protect 
Americans from these threats.
  Mr. Speaker, I encourage my colleagues to support this bill, and I 
reserve the balance of my time.
  Mrs. FLETCHER. Mr. Speaker, I yield myself such time as I may 
consume.
  Mr. Speaker, I rise in support of H.R. 8005. This legislation 
addresses the supply chains that turn illicit chemicals into 
counterfeit pills by targeting the equipment, importation, and 
production behind the fentanyl crisis. Over the past several years, we 
have worked together in a strong, bipartisan way to make real progress 
in combating the overdose crisis. However, it is important to recognize 
that an enforcement-only strategy is not the answer. This legislation 
prioritizes enforcement, and enforcement alone ultimately does not save 
lives.
  The good news is that we know what does: expanding access to 
treatment for opioid use disorder and harm-reduction interventions like 
fentanyl test strips and naloxone.
  That is why the Trump administration's actions to slash substance use 
treatment funding is so alarming. It could threaten the real progress 
that we have made. The Trump administration has dismantled the 
Substance Abuse and Mental Health Services Administration, SAMHSA, the 
agency responsible for addressing the overdose crisis, and it has kept 
hundreds of millions of dollars in addiction and overdose prevention 
funding.
  If we truly want to protect our community, we need to work together 
to increase access to treatment and stop these attacks from this 
administration.
  Mr. Speaker, I reserve the balance of my time.
  Mr. GUTHRIE. Mr. Speaker, I yield 3 minutes to the gentleman from 
Colorado (Mr. Evans), who is a tireless fighter on this issue and a 
very valuable member of the Energy and Commerce Committee.
  Mr. EVANS of Colorado. Mr. Speaker, I thank the gentleman from 
Kentucky for yielding.
  Mr. Speaker, I am proud to rise today in strong support of my bill to 
help combat the epidemic of fentanyl deaths that have been driven by 
the proliferation of counterfeit pills.
  My bill, the Stop Pills That Kill Act, is commonsense legislation 
that will help save American lives by cracking down on criminals who 
traffic poison disguised as prescription drugs.
  Under Republican leadership, the United States has thankfully seen a 
steep decline in monthly synthetic opioid deaths, driven by policies 
that strengthen border security and target cartels and drug dealers. 
Unfortunately, my State of Colorado has seen the exact opposite trend, 
with an average overdose rate of about 800 deaths per month at the end 
of 2024 increasing to 1,000 deaths now. Because Colorado's trends have 
not matched the Nation and have, in fact, gone the other direction, my 
State has, unfortunately, seen more than 1,600 tragic and preventable 
excess overdose deaths.
  I was a cop in the Denver area for over a decade. I know that this 
figure isn't just a tragic coincidence. It is a direct result of failed 
policies. While I was working to keep communities in Colorado safe from 
the poison that is fentanyl, Denver Democrats chose repeatedly to push 
soft-on-crime policies that lessened criminal sentencing for drug 
offenses while refusing to take a hard line on fentanyl.
  The Stop Pills That Kill Act counteracts these deadly policies by 
doing three simple things: It closes a sentencing loophole that allows 
poison peddlers off with a slap on the wrist. It implements 
serialization requirements for pill presses and their critical 
components. And it makes it illegal to manufacture, distribute, or 
import pill presses with the intent to illicitly produce a controlled 
substance.
  I will remind my colleagues that every 15 days under the previous 
administration we lost the same number of Americans to drug overdose 
deaths that we lost in the entirety of the September 11 terrorist 
attacks. I was a cop for 10 years, and I was a soldier for 12. I 
deployed to a combat zone as part of the global war on terror, and that 
statistic speaks volumes. We must remember the impacts that fentanyl 
has had on hundreds of thousands of American families.
  During the legislative process, two bills were folded into mine, the 
Fight Illicit Pill Presses Act, led by Representative Hageman, and the 
PRESS Act led by Representative McDowell. I thank both of them for 
their work, but I want to particularly recognize my friend, Mr. 
McDowell, who tragically lost his own brother to fentanyl nearly 10 
years ago. Representative McDowell's dedication to fighting this crisis 
is a fitting honor to his brother's legacy.
  Mr. Speaker, I urge my colleagues to join me in supporting this 
critically important, commonsense bill.
  Mrs. FLETCHER. Mr. Speaker, as we have noted, this legislation 
addresses supply chains that turn illicit chemicals into counterfeit 
pills, and it is a critical part of fighting back against the fentanyl 
crisis. We must do this and more, restoring funding, restoring 
programs, and ensuring access to treatment.
  For these reasons, Mr. Speaker, I urge my colleagues to vote ``yes'' 
on this bill, and I yield back the balance of my time.
  Mr. GUTHRIE. Mr. Speaker, I appreciate the hard work of my friend 
from Colorado. I encourage a ``yes'' vote on the bill, and I yield back 
the balance of my time.
  The SPEAKER pro tempore. The question is on the motion offered by the 
gentleman from Kentucky (Mr. Guthrie) that the House suspend the rules 
and pass the bill, H.R. 8005, as amended.
  The question was taken; and (two-thirds being in the affirmative) the 
rules were suspended and the bill, as amended, was passed.
  The title of the bill was amended so as to read: ``A bill to amend 
the Controlled Substances Act to prevent the misuse of a tableting 
machine, encapsulating machine, or critical part of a tableting and 
encapsulating machine for the illicit manufacture of a controlled 
substance or listed chemical, and for other purposes.''.
  A motion to reconsider was laid on the table.

                          ____________________