H.R. 4993House119th Congress (2025-2027)In Committee

Joe Fiandra Access to Home Infusion Act of 2025

Introduced August 19, 2025

AI-Generated Summary

Updated November 23, 2025 at 10:25 PM UTC

The Joe Fiandra Access to Home Infusion Act of 2025 changes Medicare rules to pay for external infusion pumps and certain home‑infusion drugs that patients cannot give themselves. It sets specific conditions—professional supervision, a qualified supplier, and frequent infusions—to qualify for coverage, and it requires the government to inform patients about any cost‑sharing differences.

Key Provisions

  • Adds a new rule to Medicare (title XVIII of the Social Security Act) that, starting one year after the law takes effect, will cover external infusion pumps and the associated home‑infusion drugs that are not meant to be self‑administered.
  • Coverage applies only if (1) the FDA‑approved prescribing information says the drug must be given under a health‑care professional’s supervision, (2) a qualified home‑infusion therapy supplier actually administers or supervises the infusion safely in the patient’s home, and (3) the drug is prescribed to be infused at least 12 times a year either intravenously/subcutaneously or at rates that require an external pump.
  • The Health and Human Services Secretary must make sure patients are told how their out‑of‑pocket costs for home infusion compare to other care settings.

Legislative Activity

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3 earlier actions
HouseCommittee Latest Action

Ordered to be Reported in the Nature of a Substitute (Amended) by the Yeas and Nays: 41 - 0.

December 10, 2025

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HouseIntro Referral

Introduced in House

August 19, 2025

HouseIntro Referral

Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.

August 19, 2025

HouseCommittee

Committee Consideration and Mark-up Session Held

December 10, 2025

HouseCommittee

Ordered to be Reported in the Nature of a Substitute (Amended) by the Yeas and Nays: 41 - 0.

December 10, 2025

Bill Text

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Introduced in HouseIssued August 19, 2025

I

119th CONGRESS

1st Session

H. R. 4993

IN THE HOUSE OF REPRESENTATIVES

August 19, 2025

Mr. Fitzpatrick (for himself, Mr. Dunn of Florida, and Mr. Soto) introduced the following bill; which was referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned

A BILL

To amend title XVIII of the Social Security Act to provide coverage of external infusion pumps and non-self-administrable home infusion drugs under the Medicare program.

1.

Short title

This Act may be cited as the Joe Fiandra Access to Home Infusion Act of 2025.

2.

Medicare coverage of external infusion pumps and non-self-administrable home infusion drugs

(a)

In general

Section 1861(n) of the Social Security Act (42 U.S.C. 1395x(n)) is amended by adding at the end the following new sentence:

Beginning with the first calendar quarter beginning on or after the date that is 1 year after the date of the enactment of this sentence, an external infusion pump and associated home infusion drug (as defined in subsection (iii)(3)(C)) or other associated supplies that do not meet the appropriate for use in the home requirement applied to the definition of durable medical equipment under section 414.202 of title 42, Code of Federal Regulations (or any successor to such regulation) shall be treated as meeting such requirement if each of the following criteria is satisfied:

(1)

The prescribing information approved by the Food and Drug Administration for the home infusion drug associated with the pump instructs that the drug should be administered by or under the supervision of a health care professional.

(2)

A qualified home infusion therapy supplier (as defined in subsection (iii)(3)(D)) administers or supervises the administration of the drug or biological in a safe and effective manner in the patient’s home (as defined in subsection (iii)(3)(B)).

(3)

The prescribing information described in paragraph (1) instructs that the drug should be infused at least 12 times per year—

(A)

intravenously or subcutaneously; or

(B)

at infusion rates that the Secretary determines would require the use of an external infusion pump.

.

(b)

Cost sharing notification

The Secretary of Health and Human Services shall ensure that patients are notified of the cost sharing for electing home infusion therapy compared to other applicable settings of care for the furnishing of infusion drugs under the Medicare program.