COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Congressional research reportFeb 16, 2022

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COVID-19 and Access to Medical Products:

Implications of Section 301 Tariffs

Updated February 16, 2022

Congressional Research Service

https://crsreports.congress.gov

R46954

COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Contents

Overview ......................................................................................................................................... 1

Background on Section 301 Tariffs ................................................................................................. 2

Reinstating Previously Extended Tariff Exclusions ........................................................................ 3

Medical-Care and COVID-19 Response Products .......................................................................... 4

Outlook ............................................................................................................................................ 4

Tables

Table 1. Section 301 Tariff Exclusion Extensions Granted and Under Review: MedicalCare and COVID-19 Response Products ..................................................................................... 4

Table 2. Section 301 Tariff Exclusion Extensions Under Review: Other Products With

Potential Uses For COVID-19 Response Efforts ....................................................................... 14

Contacts

Author Information........................................................................................................................ 16

COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Overview

On October 8, 2021, the Office of the U.S. Trade Representative (USTR) published a Federal

Register notice seeking comments on whether to reopen the process by which U.S. stakeholders

could apply for exclusions from Section 301 tariffs on U.S. imports from China.1 Specifically, the

agency requested comments on whether to reinstate 549 exclusions that were previously extended

and had expired or were set to expire soon.2 Some of these exclusions cover products with known

or potential medical uses related to the U.S. response to the Coronavirus Disease 2019 (COVID19) pandemic. The USTR collected comments through its portal until December 1, 2021.

Separately, in light of the spread of the COVID-19 Delta variant last summer and developments

in the production capacity of U.S.-based manufacturers to satisfy various national needs, the

USTR concluded a review of public comments on whether 99 exclusions on medical-care and/or

COVID-19 response products needed to be further extended for six months (“COVID-19

Review”).3 In response to these comments and the advice from advisory committees, the

interagency Section 301 Committee, and the White House COVID-19 Response Team, the USTR

determined on November 9, 2021, to provide a transition period for all COVID-19 exclusions set

to expire on November 14 (through November 30) and to extend 81 of the 99 COVID-19

exclusions through May 31, 2022.4 Eighty of the 99 exclusions also could potentially be

reinstated or further extended beyond May 2022 under the ongoing review process announced in

October (“General Review”).5 The agency clarified that the criteria used for granting exclusions

under the general review will be different than that applied under the COVID-19 review, and that

it may result in different effective dates for any exclusions granted.6

Some Members of Congress have raised concerns about the exclusion process.7 They have

questioned USTR’s ability to “pick winners and losers” through granting or denying requests or

have pushed for broad tariff relief amid concerns about the negative impact of tariffs on the U.S.

economy. This has been the case particularly in the aftermath of the COVID-19 pandemic, which

1 Office of the U.S. Trade Representative, “Request for Comments on the Possible Reinstatement of Certain Exclusions

in the Section 301 Investigation of China’s Acts, Policies, and Practices Related to Technology Transfer, Intellectual

Property, and Innovation,” 86 FR 56345, October 8, 2021.

2 For more detail, see Office of the U.S. Trade Representative, “Index of 549 Previously Extended Exclusions.”

3 The time window to submit comments on particular COVID-19 exclusions (“COVID-19 Review”) opened on August

27 and closed on September 27, 2021. Office of the U.S. Trade Representative, “Request for Comments on Certain

Products Exclusions Related to COVID-19: China’s Acts, Policies, and Practices Related to Technology Transfer,

Intellectual Property, and Innovation,” 86 FR 48280, August 27, 2021. The 99 COVID-19 exclusions were originally

scheduled to expire on September 30 but were temporarily extended through November 14, 2021, as the review

continued. Office of the U.S. Trade Representative, “Notice of Product Exclusion Extensions: China’s Acts, Policies,

and Practices Related to Technology Transfer, Intellectual Property, and Innovation,” 86 FR 54011, September 29,

2021.

4 Office of the U.S. Trade Representative, “Notice of Product Exclusion Extensions: China’s Acts, Policies, and

Practices Related to Technology Transfer, Intellectual Property, and Innovation,” 86 FR 63438, November 16, 2021.

5 The time window to submit comments on the reinstatement of exclusions (“General Review”) opened on October 12

and is set to close on December 1, 2021.

6 Office of the U.S. Trade Representative, “Guidance Regarding Products Covered Both in the COVID Exclusion

Notices and the Notices Concerning Possible Reinstatement of Previously Extended Exclusions.”

7 For example, Senators Ron Wyden and Thomas R. Carper, from the U.S. Senate Committee on Finance, and Senator

Tim Kaine asked the U.S. Government Accountability Office (GAO) to review how the USTR decided to exclude

products from China from tariffs under Section 301. For more detail, see GAO’s report, “U.S.-China Trade: USTR

Should Fully Document Internal Procedures for Making Tariff Exclusion and Extension Decisions,” GAO-21-506, July

28, 2021.

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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

has affected the United States’ ability to obtain certain products domestically or from countries

other than China. Other Members oppose granting any exclusions on the ground that doing so

may undermine Section 301’s effectiveness at addressing China’s unfair trade practices or hinder

U.S. efforts to incentivize domestic manufacturing of certain critical goods. The USTR’s 2021

actions were not aimed at providing broader tariff relief. They were limited to extending

unexpired exclusions on medical supplies relevant to combatting the COVID-19 pandemic and

requesting comments on whether to reinstate exclusions that were previously extended.8

This report provides a brief overview of the “General Review” as it pertains to medical products.

It also includes a list of relevant exclusions categorized by: Harmonized Tariff Schedule of the

United States (HTS) subheading, type (entire subheading or product specific), round/action (Lists

1 through 4A), expiration date, and review process (COVID-19, General, or both). For more

detail about Section 301, see CRS Report R46604, Section 301 of the Trade Act of 1974: Origin,

Evolution, and Use.

Background on Section 301 Tariffs

In 2018, the USTR determined, pursuant to an investigation under “Section 301” (Title III of the

Trade Act of 1974, 19 U.S.C. §§2411-2420), that China’s acts, policies, and practices related to

technology transfer, intellectual property (IP), and innovation were unreasonable or

discriminatory and burdened or restricted U.S. commerce. In an effort to counter these policies

and obtain their elimination, the Trump Administration imposed, under Section 301, four rounds

(Lists 1 through 4A) of increased tariffs on about two-thirds of U.S. imports from China.

However, in an effort to mitigate harm to U.S. interests, the USTR created a process whereby

interested parties could request that a particular product be excluded from the tariffs, subject to

certain criteria. Title III of the Trade Act of 1974 does not outline a formal process for exclusions

or require the USTR to establish one. The determination to do so appears to be solely at the

USTR’s discretion.

Overview of Section 301

Title III of the Trade Act of 1974 (Sections 301-310, codified at 19 U.S.C. §§2411-2420), titled “Relief from Unfair

Trade Practices," is collectively referred to as "Section 301." It grants the USTR a range of responsibilities and

authorities to impose trade sanctions on foreign countries that violate U.S. trade agreements or engage in acts

that are "unjustifiable," "unreasonable," or "discriminatory" and burden U.S. commerce. Prior to 1995, the United

States used Section 301 to unilaterally pressure other countries to eliminate trade barriers and open their markets

to U.S. exports. The creation of an enforceable dispute settlement mechanism in the World Trade Organization

(WTO), strongly supported by the United States at the time, significantly reduced the use of Section 301. While

the United States retains the flexibility to seek recourse for foreign unfair trade practices in the WTO or under

Section 301, a determination to bypass WTO dispute settlement and impose retaliatory measures in response to a

Section 301 investigation may be challenged at the WTO.

Since 2017, the USTR has launched Section 301 investigations against China, the European Union (EU), France, a

group of 10 trading partners, and Vietnam. Two investigations have resulted in the USTR imposing tariffs to date:

on U.S. imports from China and the EU. The U.S. action against the EU—unlike that against China—was based on

a WTO dispute in which the USTR anticipated being allowed to retaliate.

8 In March 2021, the USTR extended—through September 2021—the 99 exclusions granted or extended in December

2020. To provide time to review comments received between August and September 2021, the USTR adopted an

interim 45-day extension of the exclusions that were set to expire on September 30 through November 14, 2021. Office

of the U.S. Trade Representative, “Notice of Product Exclusion Extensions: China’s Acts, Policies, and Practices

Related to Technology Transfer, Intellectual Property, and Innovation,” 86 FR 13785, March 10, 2021, and “Notice of

Product Exclusion Extensions: China’s Acts, Policies, and Practices Related to Technology Transfer, Intellectual

Property, and Innovation,” 86 FR 54011, September 29, 2021.

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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

For more detail, see CRS In Focus IF11346, Section 301 of the Trade Act of 1974 and CRS Report R46604, Section

301 of the Trade Act of 1974: Origin, Evolution, and Use.

Reinstating Previously Extended Tariff Exclusions

Under the comment period and review announced in October 2021, importers and interested

parties—including law firms and trade associations—could submit comments through December

1, supporting (or opposing) the reinstatement of a specific exclusion extension, including for how

long it should be reinstated. The 549 exclusions eligible for reinstatement are reflected in 563

specially prepared product descriptions (“specific products”) or 10-digit HTS subheading

(“product categories”). Parties were not able to petition the USTR for new exclusions or

extensions to expired exclusions that were not previously extended.

The USTR indicated that it will evaluate each extension request on a case-by-case basis, taking

into account the following: (1) availability of the product in question from non-Chinese sources;

(2) attempts by the importer to source the product from the United States or third countries; (3)

the potential impact that further extensions could have in countering or eliminating China’s trade

practices covered in the Section 301 investigation; and (4) the extent to which the imposition of

Section 301 tariffs on the particular product will cause severe economic harm to the commenter

or other U.S. interests, including small businesses, employment, manufacturing output, and

critical supply chains in the United States.9

The USTR did not announce a timetable for providing responses to filed comments. However, the

agency indicated that it will publish decisions on reinstated exclusions through Federal Register

notices and that the exclusions will be retroactive to October 12, 2021. Exclusions apply

generally to specified products, so any party importing a product covered by a reinstated

exclusion may file a claim. Importers whose goods entered or were withdrawn from warehouse

for consumption on or after October 12, 2021, may request tariff refunds from U.S. Customs and

Border Protection (CBP), provided that CBP has not already calculated the final duties owed by

the time the importers file the refund claim (see text box).

Retroactive Section 301 Tariff Exclusions

Section 301 product exclusions granted by the U.S. Trade Representative (USTR) “may be retroactive for

unliquidated entries and for entries that are liquidated but where the liquidation is not final and the protest period

has not expired.

If a product exclusion has been granted, an importer of record (IOR) may request a refund by filing a corrective

action with CBP by filing a post summary correction (PSC) for unliquidated entries or file a protest for entries that

have liquidated but where the liquidation is not final and the protest period has not expired.

When a product exclusion is granted, an importer may submit a PSC to request a refund on unliquidated entries

up to 15 days prior to the scheduled liquidation date (generally within 300 days from the date of entry summary

filing). If an entry summary is set to liquidate in less than 15 days or has already liquidated, the entry summary is

beyond the PSC filing period. However, the importer may file a protest so long as the protest is filed within the

180-day period following liquidation of the impacted entry summary(ies).”

Source: U.S. Customs and Border Protection, “CSMS #42566154: Section 232 and Section 301–Extensions Requests, PSCs,

and Protests,” May 1, 2020.

9 Office of the U.S. Trade Representative, “Request for Comments on the Possible Reinstatement of Certain Exclusions

in the Section 301 Investigation of China’s Acts, Policies, and Practices Related to Technology Transfer, Intellectual

Property, and Innovation,” 86 FR 56345, October 8, 2021.

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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Medical-Care and COVID-19 Response Products

Of the 549 exclusion extensions eligible for reinstatement, CRS was able to identify 23 product

categories and 64 specific products with known medical uses (Table 1). Other exclusions eligible

for reinstatement—but not formally identified by the USTR as medical or COVID-related—may

apply to products that have potential medical uses, can serve as inputs for the manufacture of

medical products, or can be used in pandemic response efforts (see, for example, Table 2).

However, their ultimate purpose may not always be easily ascertained from HTS subheadings or

product descriptions (e.g., organic chemicals or textiles for the manufacture of pharmaceuticals or

personal protective equipment).

Outlook

In recent years, some Members have introduced legislation to amend Title III of the Trade Act of

1974, while also raising the issue of establishing or streamlining an exclusion process during

hearings and in letters to the USTR. For example, the United States Innovation and Competition

Act of 2021 (S. 1260), if enacted, would suspend tariffs—including those imposed under Section

301—on certain goods needed to combat the COVID-19 pandemic and would set out a process

for excluding imports from Section 301 tariffs in statute, rather than allow USTR to create its

own process.

The Biden Administration continues to review its trade strategy for China, thus far announcing

potential renewal of the Section 301 tariff exclusion process and focusing on enforcement of the

U.S.-China “Phase One” trade agreement.10 It is possible that the Biden Administration could use

Section 301 authorities to counter or obtain the elimination of other Chinese practices that may

disadvantage or discriminate against U.S. exports, firms, and workers in the future.

Congress may wish to engage with the Administration to develop and implement specific

guidelines for when and how to grant and extend exclusions. This has the potential to promote

transparency, consistency, and proper application of standards in reviewing exclusion requests,

thereby helping to ensure that the USTR carries out Section 301 objectives as prescribed by

Congress.

Table 1. Section 301 Tariff Exclusion Extensions Granted and Under Review: MedicalCare and COVID-19 Response Products

Type of

Exclusion

Subheading or Product

Description

2805.11.0000

Product

Specific

3401.19.0000

Entire

Subheading

HTS Code

List

Expiration

Date

Sodium metal (CAS No. 7440-23-5), in

bulk solid form

3

05/31/2022

COVID-19 &

General

Soap & other organic surface-active

products, not for toilet use, in bars,

cakes, molded pieces, and paper, etc.

impregnated or coated with soap or

detergent

4A

05/31/2022

COVID-19 &

General

Review

10 Office of the U.S. Trade Representative, “Fact Sheet: The Biden-Harris Administration’s New Approach to the U.S.-

China Trade Relationship,” Press Release, October 4, 2021.

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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Type of

Exclusion

Subheading or Product

Description

List

Expiration

Date

3401.30.5000

Product

Specific

Hand soaps and hand sanitizers in the

form of liquid or cream put up for

retail sale, other than hand sanitizers of

heading 3808

3

11/30/2021

COVID-19

3401.30.5000

Product

Specific

Disposable cloths of nonwoven textile

materials impregnated, coated or

covered with organic surface-active

preparations for washing the skin, put

up for retail sale

3

05/31/2022

COVID-19 &

General

3401.30.5000

Product

Specific

Organic surface-active liquid for

washing the skin, not containing any

aromatic or modified aromatic surfaceactive agent, put up for retail sale in a

bottle of plastics with pump-action top,

each bottle measuring not more than

17 cm in width, not more than 27 cm

in height and not more than 6.5 cm in

length and with a net weight of not

more than 0.5 kg

3

11/30/2021

COVID-19 &

General

3808.94.1000

Entire

Subheading

Disinfectants containing any aromatic

or modified aromatic disinfectant

3

05/31/2022

COVID-19

3808.94.5010

Entire

Subheading

Wipes impregnated with alcohol or

other disinfectants, other than paper

wipes or nonwoven wipes

3

05/31/2022

COVID-19

3808.94.5050

Entire

Subheading

Hydrogen peroxide put up in

disinfectant preparations for sanitizing

or disinfecting surfaces

3

11/30/2021

COVID-19

3808.94.5080

Entire

Subheading

Alcohol-based hand sanitizer

containing 60% or more by weight of

ethanol, of a kind described in

statistical note 1 to Chapter 38

3

11/30/2021

COVID-19

3808.94.5095

Entire

Subheading

Disinfectants, NESOI (described in

statistical reporting number

3808.94.5090 prior to July 1, 2021)

3

11/30/2021

COVID-19

3824.99.9297

Product

Specific

Silicon monoxide in powder form

3

05/31/2022

COVID-19 &

General

3824.99.9297

Product

Specific

Mixtures containing

N,Ndimethyldodecan-1-amine (CAS

No. 112-18-5) and N,Ndimethyltetradecan-1-amine (CAS No.

112-75-4) [*]

3

05/31/2022

COVID-19 &

General

HTS Code

Congressional Research Service

Review

5

COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Type of

Exclusion

Subheading or Product

Description

List

Expiration

Date

3917.29.0090

Product

Specific

Molded acrylonitrile-butadiene-styrene

tubes, of a kind used to effect the

sterile transfer of fluid from a bag or

vial to another container, each tube

measuring 7.5 cm or more but not

exceeding 23 cm in length, with an

inner diameter of less than 0.65 cm

and an outer diameter of less than 9

cm, one end having been angle-cut to

form a spike, and having an integrated

flange, less than 3 cm in diameter near

the spike end and removable

polyethylene caps on each end, put up

in sterile packing

2

05/31/2022

COVID-19 &

General

3917.33.0000

Product

Specific

Flexible oxygen tubes, pipes and hoses

presented with integrated molded

connectors, of polyvinyl chloride

3

05/31/2022

COVID-19

3917.33.0000

Product

Specific

Flexible gas sampling tubes, pipes and

hoses, of polyvinyl chloride, with lock

connectors at each end

3

05/31/2022

COVID-19

3919.90.5060

Product

Specific

Polyethylene film, 20.32 to 198.12 cm

in width, and 30.5 to 2000.5 m in

length, coated on one side with solvent

acrylic adhesive, clear or in transparent

colors, whether or not printed, in rolls

2

11/30/2021

COVID-19 &

General

3920.10.0000

Product

Specific

Rectangular sheets of high-density or

low-density polyethylene, 111.75 cm to

215.9 cm in width, and 152.4 cm to

304.8 cm in length, with a sticker

attached to mark the center of each

sheet, of a kind used in hospital or

surgery center operating rooms

2

05/31/2022

COVID-19 &

General

3921.19.0000

Product

Specific

Sheets and strips consisting of both

cross-linked polyethylene and ethylene

vinyl acetate, of a width greater than 1

m but not greater than 1.5 m, and a

length greater than 1.75 m but not

greater than 2.6 m

2

05/31/2022

COVID-19 &

General

3921.90.1500

Product

Specific

Polyethylene sheet and film laminated

with spunbond-spunbond-spunbond

nonwoven polypropylene fabric,

measuring 1.12 m or more but not

over 1.52 m in width and 1.93 m or

more but not over 2.29 m in length,

and weighing 55 g/m² or more but not

exceeding 88 g/m²

2

05/31/2022

COVID-19 &

General

3923.10.9000

Product

Specific

Container units of plastics, each

comprising a tub and lid therefore,

configured or fitted for the

conveyance, packing, or dispensing of

wet wipes

3

05/31/2022

COVID-19 &

General

HTS Code

Congressional Research Service

Review

6

COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Type of

Exclusion

Subheading or Product

Description

List

Expiration

Date

3923.21.0030

Product

Specific

Sacks and bags of polymers of

ethylene, reclosable, qualifying as Class

1 medical devices by the U.S. Food and

Drug Administration under product

code NNI

3

05/31/2022

COVID-19

3923.21.0095

Entire

Subheading

Sacks and bags of polymers of

ethylene, NESOI

3

05/31/2022

COVID-19 &

General

3923.50.0000

Product

Specific

Injection molded polypropylene plastic

caps or lids each weighing not over 24

grams designed for dispensing wet

wipes

3

05/31/2022

COVID-19 &

General

3926.20.9010

Product

Specific

Aprons, of plastic, of a kind used as

personal protective equipment

3

11/30/2021

COVID-19

3926.20.9050

Entire

Subheading

Articles of apparel & clothing

accessories, of plastic, NESOI

3

05/31/2022

COVID-19 &

General

3926.90.9910

Entire

Subheading

Laboratory ware

4A

05/31/2022

COVID-19 &

General

3926.90.9950

Product

Specific

Face shields of transparent plastics,

whether or not assembled

4A

05/31/2022

COVID-19

3926.90.9985

Product

Specific

Bowls of molded plastics, with clips for

retaining guide wires during surgical

procedures (described in statistical

reporting number 3926.90.9990 prior

to July 1, 2020)

4A

05/31/2022

COVID-19 &

General

3926.90.9985

Product

Specific

Disposable graduated medicine

dispensing cups of plastics (described

in statistical reporting number

3926.90.9990 prior to July 1, 2020)

4A

05/31/2022

COVID-19 &

General

3926.90.9985

Product

Specific

Single-use sterile drapes and covers of

plastics, of a kind used to protect the

sterile field in surgical operating rooms

(described in statistical reporting

number 3926.90.9990 prior to July 1,

2020)

4A

05/31/2022

COVID-19 &

General

3926.90.9985

Product

Specific

Sterile decanters of polystyrene

plastics, each of a kind used to transfer

aseptic fluids or medication to and

from sterile bags, vials or glass

containers (described in statistical

reporting number 3926.90.9990 prior

to July 1, 2020)

4A

05/31/2022

COVID-19 &

General

3926.90.9985

Product

Specific

Coverings, of plastics, designed to fit

over wound sites or casts thereby

forming a protective seal for keeping

the covered area dry and debris free

while showering or bathing (described

in statistical reporting number

3926.90.9990 prior to July 1, 2020)

4A

05/31/2022

COVID-19 &

General

4015.19.0510

Entire

Subheading

Medical gloves, mittens and mitts of

natural rubber, other than hard rubber

4A

11/30/2021

COVID-19 &

General

HTS Code

Congressional Research Service

Review

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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Type of

Exclusion

Subheading or Product

Description

List

Expiration

Date

4015.19.0550

Entire

Subheading

Medical gloves, of vulcanized rubber

other than hard rubber, NESOI

4A

11/30/2021

COVID-19 &

General

4015.19.1010

Entire

Subheading

Seamless, disposable gloves, of

vulcanized rubber other than hard

rubber

3

11/30/2021

COVID-19 &

General

4015.19.1010

Product

Specific

Seamless disposable gloves of

acrylonitrile butadiene rubber, other

than for surgical or medical use

3

11/30/2021

COVID-19 &

General

4015.19.1010

Product

Specific

Seamless disposable gloves of natural

rubber latex, other than for surgical or

medical use

3

11/30/2021

COVID-19 &

General

4818.90.0020

Entire

Subheading

Face masks of paper pulp, paper

cellulose wadding or webs of cellulose

fibers

4A

05/31/2022

COVID-19 &

General

4818.90.0080

Entire

Subheading

Bed sheets and similar household or

hospital articles of paper pulp, paper

cellulose wadding or webs of cellulose

fibers, NESOI

4A

05/31/2022

COVID-19 &

General

4819.50.4060

Entire

Subheading

Packing containers, NESOI, of paper,

paperboard, cellulose wadding or webs

of cellulose fibers

3

05/31/2022

COVID-19 &

General

5210.11.4040

Entire

Subheading

Woven fabrics of cotton, containing

less than 85 percent by weight of

cotton, mixed mainly or solely with

man-made fibers, weighing not more

than 200 g/m2, unbleached, Plain

Weave, of number 42 or lower

number, sheeting

4A

05/31/2022

COVID-19 &

General

5210.11.6020

Entire

Subheading

Woven fabrics of cotton, containing

less than 85 percent by weight of

cotton, mixed mainly or solely with

man-made fibers, weighing not more

than 200 g/m2, unbleached, plain

weave, of numbers 43 to 68, poplin or

broadcloth

4A

05/31/2022

COVID-19 &

General

5504.10.0000

Entire

Subheading

Artificial staple fibers, not carded,

combed or otherwise processed for

spinning: of viscose rayon

3

05/31/2022

COVID-19 &

General

5603.12.0090

Entire

Subheading

Nonwovens, whether or not

impregnated, coated, covered or

laminated, of man-made filaments,

weighing more than 25 g/m2 but not

more than 70 g/m2, other

3

05/31/2022

COVID-19 &

General

HTS Code

Congressional Research Service

Review

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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Type of

Exclusion

Subheading or Product

Description

List

Expiration

Date

5603.12.0090

Product

Specific

Nonwoven fabrics of man-made fibers,

weighing more than 25 g/m2 but not

more than 70 g/m2, with a smooth or

embossed texture (not impregnated,

coated or covered with material other

than or in addition to rubber, plastics,

wood pulp or glass fibers), in rolls that

are pre-slitted in lengths of not less

than 15 cm to not more than 107 cm,

for use in the manufacture of personal

care wipes

3

11/30/2021

COVID-19 &

General

5603.14.9090

Entire

Subheading

Other nonwovens, whether or not

impregnated, coated, covered or

laminated, of man-made filaments,

weighing more than 150 g/m2, other

than laminated fabrics, not

impregnated, coated or covered with

material other than or in addition to

rubber, plastics, wood pulp or glass

fibers

3

05/31/2022

COVID-19 &

General

5603.92.0090

Entire

Subheading

Other non-woven fabrics, not manmade, other than floor covering

underlays & laminated fabrics, not

impregnated, coated, or covered,

weighing more than 25 g/m2 and less

than 70 g/m2

3

05/31/2022

COVID-19 &

General

5603.93.0090

Entire

Subheading

Other non-woven fabrics, not manmade, other than floor covering

underlays & laminated fabrics, not

impregnated, covered, weighing more

than 70 g/m2 and less than 150 g/m2

3

05/31/2022

COVID-19 &

General

6116.10.6500

Product

Specific

Gloves, containing less than 50% by

weight of textile fibers, coated with

rubber or plastics designed for

enhanced grip

3

11/30/2021

COVID-19 &

General

6210.10.5010

Entire

Subheading

Surgical or isolation gowns, disposable,

of nonwoven fabrics of heading 5602

or 5603

4A

05/31/2022

COVID-19 &

General

6210.10.5090

Entire

Subheading

Disposable apparel designed for use in

hospitals, clinics, laboratories and

other areas, of nonwoven fabrics of

heading 5602 or 5603, NESOI

4A

05/31/2022

COVID-19 &

General

6307.90.6090

Entire

Subheading

Other made up articles, including dress

patterns: surgical drapes, of fabric

formed on a base of paper or covered

with paper, other

4A

11/30/2021

COVID-19 &

General

6307.90.6800

Entire

Subheading

Other made up articles, including dress

patterns: surgical drapes of spun laced

or bonded fiber fabric disposable

surgical drapes of man-made fibers

4A

11/30/2021

COVID-19 &

General

HTS Code

Congressional Research Service

Review

9

COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Type of

Exclusion

Subheading or Product

Description

List

Expiration

Date

6307.90.7200

Entire

Subheading

Other made up articles, including dress

patterns: surgical drapes, NESOI, not

spun laced or bonded fiber fabric.

4A

05/31/2022

COVID-19

6307.90.9845

Product

Specific

Face masks and particulate facepiece

respirators, of textile fabrics

(described in statistical reporting

number 6307.90.9889 prior to July 1,

2020)

4A

11/30/2021

COVID-19 &

General

6307.90.9845

Product

Specific

Single-use medical masks of textile

material (described in statistical

reporting number 6307.90.9889 prior

to July 1, 2020)

4A

11/30/2021

COVID-19 &

General

6307.90.9850

Product

Specific

Face masks and particulate facepiece

respirators, of textile fabrics

(described in statistical reporting

number 6307.90.9889 prior to July 1,

2020)

4A

11/30/2021

COVID-19 &

General

6307.90.9850

Product

Specific

Single-use medical masks of textile

material (described in statistical

reporting number 6307.90.9889 prior

to July 1, 2020)

4A

11/30/2021

COVID-19 &

General

6307.90.9870

Product

Specific

Face masks and particulate facepiece

respirators, of textile fabrics

(described in statistical reporting

number 6307.90.9889 prior to July 1,

2020)

4A

11/30/2021

COVID-19 &

General

6307.90.9870

Product

Specific

Single-use medical masks of textile

material (described in statistical

reporting number 6307.90.9889 prior

to July 1, 2020)

4A

11/30/2021

COVID-19 &

General

6307.90.9875

Product

Specific

Face masks and particulate facepiece

respirators, of textile fabrics

(described in statistical reporting

number 6307.90.9889 prior to July 1,

2020)

4A

11/30/2021

COVID-19 &

General

6307.90.9891

Product

Specific

Cold packs consisting of a single-use,

instant, endothermic chemical reaction

cold pack combined with a textile

exterior lining (described in statistical

reporting number 6307.90.9889 prior

to July 1, 2020)

4A

05/31/2022

COVID-19 &

General

6307.90.9891

Product

Specific

Disposable shoe and boot covers of

man-made fiber fabrics (described in

statistical reporting number

6307.90.9889 prior to July 1, 2020)

4A

11/30/2021

COVID-19 &

General

6307.90.9891

Product

Specific

Hot packs of textile material, singleuse (described in statistical reporting

number 6307.90.9889 prior to July 1,

2020)

4A

05/31/2022

COVID-19 &

General

HTS Code

Congressional Research Service

Review

10

COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Type of

Exclusion

Subheading or Product

Description

List

Expiration

Date

6307.90.9891

Product

Specific

Laparotomy sponges of cotton

(described in statistical reporting

number 6307.90.9889 prior to July 1,

2020)

4A

05/31/2022

COVID-19 &

General

6307.90.9891

Product

Specific

Single-use blood pressure cuff sleeves

of textile materials (described in

statistical reporting number

6307.90.9889 prior to July 1, 2020)

4A

05/31/2022

COVID-19 &

General

6307.90.9891

Product

Specific

Single-use stethoscope covers

(described in statistical reporting

number 6307.90.9889 prior to July 1,

2020)

4A

05/31/2022

COVID-19 &

General

6307.90.9891

Product

Specific

Woven gauze sponges of cotton in

square or rectangular sizes (described

in statistical reporting number

6307.90.9889 prior to July 1, 2020)

4A

05/31/2022

COVID-19 &

General

6505.00.8015

Entire

Subheading

Nonwoven disposable headgear

without peaks or visors of manmade

fibers

3

05/31/2022

COVID-19 &

General

8413.20.0000

Product

Specific

Hand pumps (other than for fuel or

lubricants, not fitted or designed to be

fitted with a metering device), each

used to dispense a metered quantity of

liquid soap or sanitizer

3

05/31/2022

COVID-19 &

General

8413.20.0000

Product

Specific

Hand pumps for liquids of acrylonitrile

butadiene styrene plastics

3

05/31/2022

COVID-19 &

General

8421.39.8090

Product

Specific

Disposable plastic filters of a kind

suitable for filtering and dehumidifying

a patient’s breath in a medical device

such as a gas analyzer

1

05/31/2022

COVID-19 &

General

8424.89.9000

Product

Specific

Dispensers of hand-cleaning or handsanitizing solutions, whether employing

a manual pump or a proximitydetecting battery-operated pump, each

article weighing not more than 3 kg

2

05/31/2022

COVID-19 &

General

8424.90.9080

Entire

Subheading

Parts of mechanical appliances for

projecting, dispersing, spraying

liquid/powder; spray guns and similar

appliances, NESOI

3

05/31/2022

COVID-19 &

General

8531.20.0040

Product

Specific

Indicator panels incorporating LEDs,

designed for use in medical infusion

equipment

3

05/31/2022

COVID-19 &

General

8537.10.9170

Product

Specific

Data input devices each with display

capabilities of a kind used for magnetic

resonance imaging equipment,

computed tomography equipment,

intraoperative X-ray equipment or

patient monitors

3

05/31/2022

COVID-19

HTS Code

Congressional Research Service

Review

11

COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Type of

Exclusion

Subheading or Product

Description

List

Expiration

Date

8543.10.0000

Product

Specific

S-band and X-band linear accelerators

designed for use in radiation surgery

or radiation therapy equipment

1

05/31/2022

COVID-19 &

General

9004.90.0010

Product

Specific

Protective articles (described in

statistical reporting number

9004.90.0000 prior to January 1, 2021)

4A

05/31/2022

COVID-19 &

General

9004.90.0090

Product

Specific

Protective articles (described in

statistical reporting number

9004.90.0000 prior to January 1, 2021)

4A

05/31/2022

COVID-19 &

General

9011.80.0000

Product

Specific

Compound binocular optical

microscopes (other than stereoscopic

microscopes and microscopes for

photomicrography, cinemicrography or

microprojection), each with

magnification of 40X or more but not

exceeding 1,000X, weighing not more

than 3 kg

3

05/31/2022

COVID-19 &

General

9011.80.0000

Product

Specific

Compound optical microscopes (other

than stereoscopic microscopes and

microscopes for photomicrography,

cinemicrography or microprojection),

each with magnification of 40X or

more but not exceeding 400X,

weighing not more than 15 kg

3

05/31/2022

COVID-19 &

General

9018.11.9000

Product

Specific

Disposable electrocardiograph

electrodes

1

05/31/2022

COVID-19 &

General

9018.12.0000

Product

Specific

Ultrasonic scanning apparatus, each

having dimensions not exceeding 122

cm by 77 cm by 127 cm, whether or

not presented with transducer

1

05/31/2022

COVID-19

9018.19.9530

Product

Specific

Blood pressure monitors suitable for

use by medical professionals

1

05/31/2022

COVID-19

9018.19.9550

Product

Specific

Digital peak flow meters suitable for

use by medical professionals

1

05/31/2022

COVID-19 &

General

9018.19.9550

Product

Specific

Fingertip pulse oximeters suitable for

use by medical professionals

1

05/31/2022

COVID-19 &

General

9018.19.9560

Product

Specific

Disposable surface electrodes for

Intra-operative neuromonitoring

systems, each composed of a surface

electrode pad, an insulated wire, and a

standard DIN 42802 connector

1

05/31/2022

COVID-19 &

General

9018.19.9560

Product

Specific

Bismuth germanate crystals with set

dimensional and surface finish

requirements and used as a detection

element in Positron Emission

Tomography detectors

1

05/31/2022

COVID-19 &

General

9018.19.9560

Product

Specific

Magnetic resonance imaging patient

enclosure devices, each incorporating

radio frequency and gradient coils

1

05/31/2022

COVID-19 &

General

HTS Code

Congressional Research Service

Review

12

COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Type of

Exclusion

Subheading or Product

Description

List

Expiration

Date

9018.19.9560

Product

Specific

Parts and accessories of capnography

monitors

1

05/31/2022

COVID-19 &

General

9018.90.2000

Product

Specific

Otoscopes

1

05/31/2022

COVID-19 &

General

9018.90.3000

Product

Specific

Anesthetic instruments and appliances

suitable for use in medical or surgical

sciences, and parts and accessories of

the foregoing

1

05/31/2022

COVID-19

9018.90.3000

Product

Specific

Anesthesia masks

1

05/31/2022

COVID-19 &

General

9018.90.6000

Product

Specific

Electrosurgical cautery pencils with

electrical connectors

1

05/31/2022

COVID-19 &

General

9018.90.7580

Product

Specific

Printed circuit board assemblies

designed for use in displaying

operational performance of medical

infusion equipment

1

05/31/2022

COVID-19 &

General

9022.12.0000

Product

Specific

Combined positron emission

tomography/computed tomography

scanners which utilize multiple PET

gantries on a common base

1

05/31/2022

COVID-19 &

General

9022.90.2500

Product

Specific

X-ray tables

1

05/31/2022

COVID-19 &

General

9022.90.4000

Product

Specific

X-ray tube housings and parts thereof

1

05/31/2022

COVID-19 &

General

9022.90.6000

Product

Specific

Multi-leaf collimators of radiotherapy

systems based on the use of X-ray

1

05/31/2022

COVID-19 &

General

9022.90.6000

Product

Specific

Parts and accessories, of metal, for

mobile X-ray apparatus

1

05/31/2022

COVID-19 &

General

9022.90.6000

Product

Specific

Vertical stands specially designed to

support, contain or adjust the

movement of X-ray digital detectors,

or the X-ray tube and collimator in

complete X-ray diagnostic systems

1

05/31/2022

COVID-19 &

General

9022.90.9500

Product

Specific

Thermoplastic masks of

polycaprolactone for the use of

immobilizing patients, during the use of

alpha, beta or gamma radiations, for

radiography or radiotherapy

1

05/31/2022

COVID-19 &

General

9025.19.8010

Entire

Subheading

Clinical infrared thermometers of a

kind described in statistical note 2, not

combined with other instruments

2

05/31/2022

COVID-19

9025.19.8020

Entire

Subheading

Clinical thermometers, other than

infrared, not combined with other

instruments, NESOI

2

05/31/2022

COVID-19

9025.19.8060

Entire

Subheading

Infrared thermometers, other than

clinical, not combined with other

instruments, NESOI

2

05/31/2022

COVID-19

HTS Code

Congressional Research Service

Review

13

COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

HTS Code

Type of

Exclusion

Subheading or Product

Description

List

Expiration

Date

Review

9025.19.8085

Entire

Subheading

Thermometers, not combined with

other instruments, NESOI

2

05/31/2022

COVID-19

9027.90.5650

Product

Specific

Inoculator sets of plastics, each

consisting of a plate with multiple

wells, a display tray, and a lid; when

assembled, the set measuring 105 mm

or more but not exceeding 108 mm in

width, 138 mm or more but not

exceeding 140 mm in depth, and 6.5

mm or less in thickness

1

05/31/2022

COVID-19 &

General

Source: Congressional Research Service and the Office of the U.S. Trade Representative.

Notes: NESOI: not elsewhere specified or included. Products covered by Lists 1 through 3 are subject to

additional Section 301 tariffs (ad valorem) of 25%, while those under List 4A are subject to a 7.5% additional tariff.

The time window to submit comments as part of the “COVID-19 Review” opened on August 27 and closed on

September 27, 2021, while the comment window for the “General Review” opened on October 12 and is to

close on December 1, 2021. The 99 exclusions expiring on November 30, 2021, are reflected in 84 specially

prepared product descriptions and 33 10-digit Harmonized Tariff Schedule of the United States (HTS)

subheadings. [*] In October 2020, the USTR made a technical amendment to this product specific exclusion. Its

original description was “‘Mixtures containing 2-(dimethylamino) ethanol (CAS No. 108–01–0).” For more detail,

see Office of the U.S. Trade Representative, “Notice of Product Exclusion Extension Amendments: China’s Acts,

Policies, and Practices Related to Technology Transfer, Intellectual Property, and Innovation,” 85 FR 63332,

October 7, 2020.

Table 2. Section 301 Tariff Exclusion Extensions Under Review: Other Products With

Potential Uses For COVID-19 Response Efforts

Type of

Exclusion

Subheading or Product

Description

8409.91.9990

Product

Specific

Hydraulic valve lifters of steel with

rollers, suitable for use solely or

principally with spark-ignition internal

combustion piston engines (other than

for aircraft engines, marine propulsion

engines or for vehicles of subheading

8701.20, or headings 8702, 8703 or

8704), each measuring 5 cm or more

but not over 13 cm in length and 2.5

cm or more but not over 3.9 cm in

diameter and weighing 135 g or more

but not over 410 g [e.g., for

ambulances]

3

Expired

(12/31/2020)

General

8409.91.9990

Product

Specific

Solid valve lifters of steel, suitable for

use solely or principally with sparkignition internal combustion piston

engines (other than for aircraft

engines, marine propulsion engines or

for vehicles of subheading 8701.20, or

headings 8702, 8703 or 8704), each

measuring 19 mm or more but not

over 114 mm in length and 6 mm or

more but not over 26 mm in diameter

and weighing 20 g or more but not

over 250 g [e.g., for ambulances]

3

Expired

(12/31/2020)

General

HTS Code

Congressional Research Service

List

Expiration

Date

Review

14

COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Type of

Exclusion

Subheading or Product

Description

8413.30.9090

Product

Specific

Cooling medium pumps for internal

combustion piston engines of the

motor vehicles of headings 8703 or

8704 [e.g., for ambulances]

3

Expired

(12/31/2020)

General

8421.39.8015

Product

Specific

Air purification equipment, electrically

powered, weighing less than 36 kg

1

Expired

(12/31/2020)

General

9011.10.8000

Product

Specific

Stereoscopic microscopes, not

provided with a means for

photographing the image, valued not

over $500 per unit

1

Expired

(12/31/2020)

General

9011.90.0000

Product

Specific

Adapter rings, tubes and extension

sleeves, stands and arm assemblies,

stages and gliding tables, eye guards

and focusing racks, all the foregoing

designed for use with compound

optical microscopes

1

Expired

(12/31/2020)

General

9018.12.0000

Product

Specific

Portable ultrasonic scanner consoles,

each weighing less than 4 kg,

presented with or without transducer

1

Expired

(12/31/2020)

General

9022.14.0000

Product

Specific

Radiation therapy systems, each

encased by steel-based structural shell

with gantry cover comprising three

pairs of plastics-based panels

1

Expired

(12/27/2020)

General

9022.90.6000

Product

Specific

Printed circuit board assemblies, of a

kind designed for use in X-ray

apparatus

1

Expired

(12/31/2020)

General

9025.19.8010

Product

Specific

Digital clinical thermometers

(described in statistical reporting

number 9025.19.8040 prior to July 1,

2020)

2

Expired

(12/31/2020)

General

9025.19.8010

Product

Specific

Digital clinical thermometers, valued

not over $11 each (described in

statistical reporting number

9025.19.8040 prior to July 1, 2020)

2

Expired

(12/31/2020)

General

9025.19.8020

Product

Specific

Digital clinical thermometers

(described in statistical reporting

number 9025.19.8040 prior to July 1,

2020)

2

Expired

(12/31/2020)

General

9025.19.8020

Product

Specific

Digital clinical thermometers, valued

not over $11 each (described in

statistical reporting number

9025.19.8040 prior to July 1, 2020)

2

Expired

(12/31/2020)

General

9403.90.8041

Product

Specific

Bed rails, each of which attaches to

the side of a bed to prevent the

occupant of the bed from rolling out,

with a nylon mesh fabric cover

3

Expired

(12/31/2020)

General

HTS Code

List

Expiration

Date

Review

Source: Congressional Research Service and the Office of the U.S. Trade Representative.

Notes: Products covered by Lists 1 through 3 are subject to additional Section 301 tariffs (ad valorem) of 25%.

The time window to submit comments as part of the “General Review” opened on October 12 and is to close

on December 1, 2021.

Congressional Research Service

15

COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs

Author Information

Andres B. Schwarzenberg

Analyst in International Trade and Finance

Disclaimer

This document was prepared by the Congressional Research Service (CRS). CRS serves as nonpartisan

shared staff to congressional committees and Members of Congress. It operates solely at the behest of and

under the direction of Congress. Information in a CRS Report should not be relied upon for purposes other

than public understanding of information that has been provided by CRS to Members of Congress in

connection with CRS’s institutional role. CRS Reports, as a work of the United States Government, are not

subject to copyright protection in the United States. Any CRS Report may be reproduced and distributed in

its entirety without permission from CRS. However, as a CRS Report may include copyrighted images or

material from a third party, you may need to obtain the permission of the copyright holder if you wish to

copy or otherwise use copyrighted material.

Congressional Research Service

R46954 · VERSION 5 · UPDATED

16

This is a copy of a public record, reproduced as it was published. It is not legal advice, and it may not be the version a court would rely on. Check the official source before you cite it.

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