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II
117TH CONGRESS
1ST SESSION
S. 1334
To amend the Toxic Substances Control Act to codify a Federal cause of
action and a type of remedy available for individuals significantly exposed
to per- and polyfluoroalkyl substances, to encourage research and ac-
countability for irresponsible discharge of those substances, and for other
purposes.
IN THE SENATE OF THE UNITED STATES
APRIL 22, 2021
Mrs. GILLIBRAND introduced the following bill; which was read twice and
referred to the Committee on Environment and Public Works
A BILL
To amend the Toxic Substances Control Act to codify a
Federal cause of action and a type of remedy available
for individuals significantly exposed to per- and
polyfluoroalkyl substances, to encourage research and ac-
countability for irresponsible discharge of those sub-
stances, and for other purposes.
Be it enacted by the Senate and House of Representa-
1
tives of the United States of America in Congress assembled,
2
SECTION 1. SHORT TITLE.
3
This Act may be cited as the ββPFAS Accountability
4
Act of 2021ββ.
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β’S 1334 IS
SEC. 2. FINDINGS.
1
Congress finds thatβ
2
(1) the Centers for Disease Control and Preven-
3
tion has detected numerous perfluoroalkyl and
4
polyfluoroalkyl substances (referred to in this Act as
5
ββPFASββ) in the blood serum of individuals in the
6
United States, all of which come from manufac-
7
turing and use of PFAS by humans, as there is no
8
natural source of PFAS in human blood;
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(2) peer-reviewed studies by other organizations
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have detected PFAS in the drinking water of at
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least 200,000,000 individuals in the United States;
12
(3) PFAS are introduced into the market every
13
year, and little research is conducted to ensure the
14
safety of PFAS for individuals;
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(4) as of the day before the date of enactment
16
of this Act, a Federal statutory cause of action does
17
not exist for individuals harmed by the long-term ef-
18
fects of PFAS exposure; and
19
(5) PFAS exposure, even at low levels, has been
20
linked to chronic diseases, including cancer, repro-
21
ductive and developmental harms, and harms to the
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immune system.
23
SEC. 3. PURPOSES.
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The purposes of this Act areβ
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β’S 1334 IS
(1) to encourage PFAS research and provide
1
accountability for irresponsible PFAS manufacturing
2
and irresponsible use of PFAS in manufacturing by
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codifyingβ
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(A) a Federal cause of action for individ-
5
uals significantly exposed to PFAS; and
6
(B) a medical monitoring remedy for those
7
individuals;
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(2) to help address harm to individuals signifi-
9
cantly exposed to PFAS byβ
10
(A) codifying that harm as an injury at
11
law and equity; and
12
(B) shifting the costs of medical moni-
13
toring from those individuals to the parties re-
14
sponsible for the exposure; and
15
(3) to provide incentives for industry to fund
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PFAS safety research.
17
SEC. 4. CAUSE OF ACTION AND REMEDIES.
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(a) IN GENERAL.βThe Toxic Substances Control Act
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is amended by inserting after section 24 (15 U.S.C. 2623)
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the following:
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β’S 1334 IS
ββSEC. 25. INDIVIDUALS EXPOSED TO PERFLUOROALKYL
1
AND POLYFLUOROALKYL SUBSTANCES.
2
ββ(a) DEFINITION OF PFAS.βIn this section, the
3
term βPFASβ means a perfluoroalkyl or polyfluoroalkyl
4
substance with at least 1 fully fluorinated carbon atom.
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ββ(b) CAUSE OF ACTION.βAn individual who is sig-
6
nificantly exposed to PFAS or has reasonable grounds to
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suspect that the individual was significantly exposed to
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PFAS may bring a claim, individually or on behalf of a
9
class of similarly situated individuals, in any district court
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of the United States for appropriate legal and equitable
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relief against any person thatβ
12
ββ(1) engaged in any portion of a manufacturing
13
process that created the PFAS to which the indi-
14
vidual was significantly exposed, including any
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telomer, fluorosurfactant, or toll manufacturing
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process leading to the creation of the PFAS to
17
which the individual was significantly exposed; and
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ββ(2) foresaw or reasonably should have foreseen
19
that the creation or use of PFAS would result in
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human exposure to PFAS.
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ββ(c) MEDICAL MONITORING.β
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ββ(1) IN GENERAL.βA court may award medical
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monitoring to an individual or class of individuals
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bringing a claim under subsection (b) ifβ
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β’S 1334 IS
ββ(A) the individual or class has been sig-
1
nificantly exposed to PFAS;
2
ββ(B) as a result of that exposure, the indi-
3
vidual or class has suffered an increased risk of
4
developing a disease associated with exposure to
5
PFAS;
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ββ(C) as a result of that increased risk,
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there is a reasonable basis for the individual or
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class to undergo periodic diagnostic medical ex-
9
aminations of a nature or frequency that is dif-
10
ferent from or additional to what would be pre-
11
scribed in the absence of the exposure; and
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ββ(D) those medical examinations are effec-
13
tive in detecting a disease associated with expo-
14
sure to PFAS.
15
ββ(2) PRESUMPTION
OF
SIGNIFICANT
EXPO-
16
SURE.β
17
ββ(A) INDIVIDUALS.βAn individual plain-
18
tiff shall be presumed to have been significantly
19
exposed to PFAS under paragraph (1)(A) if the
20
individualβ
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ββ(i) demonstrates thatβ
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ββ(I) the defendant engaged in
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any portion of a manufacturing proc-
24
ess that created the PFAS to which
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β’S 1334 IS
the individual was significantly ex-
1
posed, including any telomer, fluoro-
2
surfactant, or toll manufacturing pro-
3
cess leading to the creation of the
4
PFAS to which the individual was sig-
5
nificantly exposed; and
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ββ(II) the PFAS described in sub-
7
clause (I) were released into 1 or
8
more areas where the individual would
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have been exposed for a cumulative
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period of not less than 1 year; or
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ββ(ii) offers testing results that dem-
12
onstrate that PFAS or metabolites of
13
PFAS have been or are currently detected
14
in the body or blood serum of the indi-
15
vidual.
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ββ(B) CLASS ACTIONS.βIn a class action, a
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presumption of significant exposure to PFAS
18
under paragraph (1)(A) shall be established for
19
the class byβ
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ββ(i) demonstrating thatβ
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ββ(I) the defendant engaged in
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any portion of a manufacturing proc-
23
ess that created the PFAS to which
24
the class members were significantly
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β’S 1334 IS
exposed, including any telomer, fluoro-
1
surfactant, or toll manufacturing pro-
2
cess leading to the creation of the
3
PFAS to which the class members
4
were significantly exposed; and
5
ββ(II) the PFAS described in sub-
6
clause (I) were released into 1 or
7
more areas where a representative
8
portion of the class members would
9
have been exposed for a cumulative
10
period of not less than 1 year; or
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ββ(ii) offering testing results that dem-
12
onstrate that PFAS or metabolites of
13
PFAS have been or are currently detected
14
in the bodies of a representative portion of
15
class members that share sufficient com-
16
mon exposure characteristics with the
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class.
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ββ(3) REBUTTING THE PRESUMPTION.β
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ββ(A) IN
GENERAL.βA defendant may
20
rebut a presumption of significant exposure
21
with respect to an individual plaintiff or class
22
member for which testing results are not of-
23
fered under subparagraph (A)(ii) or (B)(ii) of
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β’S 1334 IS
paragraph (2) by offering results for that indi-
1
vidual or class member of testing thatβ
2
ββ(i) uses a generally accepted method
3
for detecting the particular PFAS or me-
4
tabolites of PFAS at issue;
5
ββ(ii) is performed by an independent
6
provider agreed on by both parties; and
7
ββ(iii) confirms that the relevant PFAS
8
or metabolites of PFAS likely were not
9
present in the body of the individual or
10
class member at the relevant time in a suf-
11
ficient quantity to qualify as significant ex-
12
posure under paragraph (1)(A).
13
ββ(B) COSTS.βA defendant shall be re-
14
sponsible for the costs of testing under subpara-
15
graph (A).
16
ββ(C) INDEPENDENT
PROVIDER.βIf both
17
parties cannot agree on an independent pro-
18
vider under subparagraph (A)(ii), the court
19
shall appoint an independent provider.
20
ββ(4) INCREASED
RISK
OF
DEVELOPING
DIS-
21
EASE.β
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ββ(A) IN GENERAL.βIf there is insufficient
23
toxicological data to reasonably determine
24
whether an individual or class has suffered an
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β’S 1334 IS
increased risk of developing a disease associated
1
with exposure to any individual PFAS or group
2
of PFAS under paragraph (1)(B), a court may
3
lower the standard for scientific proof with re-
4
gard to the increased risk of developing that
5
disease until independent and reliable toxi-
6
cological data is available with respect to that
7
individual PFAS or group of PFAS.
8
ββ(B) ORDERING STUDIES.βTo make avail-
9
able independent and reliable toxicological data
10
described in subparagraph (A) with respect to
11
an individual PFAS or group of PFAS, a court
12
may order new or additional epidemiological,
13
toxicological, or other studies or investigations
14
of that individual PFAS or group of PFAS as
15
part of a medical monitoring remedy awarded
16
under paragraph (1).
17
ββ(d) SENSE OF CONGRESS.βIt is the sense of Con-
18
gress that courts should encourage more reliable and inde-
19
pendent research into the latent health effects of PFAS.
20
ββ(e) EFFECT ON STATE LAW CLAIMS AND REM-
21
EDIES.βNothing in this sectionβ
22
ββ(1) preempts, alters, bars, or precludes any
23
State law claims or remedies, including any State
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β’S 1334 IS
law claims or remedies for an injury addressed by
1
this section; or
2
ββ(2) provides an exclusive claim or remedy.ββ.
3
(b) CLERICAL AMENDMENT.βThe table of contents
4
for the Toxic Substances Control Act (Public Law 94β
5
469; 90 Stat. 2003) is amended by inserting after the item
6
relating to section 24 the following:
7
ββSec. 25. Individuals exposed to perfluoroalkyl and polyfluoroalkyl sub-
stances.ββ.
Γ
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