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HR 4993 Cleared committee

Allows Medicare to cover external infusion pumps and home infusion drugs that do not meet its usual home-use test, when the drug is given under a health professional's supervision and a qualified home infusion supplier provides it.

Official title: Joe Fiandra Access to Home Infusion Act of 2025

Next stop House floor: awaiting a vote
Timeline each lane is a chamber; dates pull from congress.gov actions
House
Introduced 19-AUG-2025
Referred 19-AUG-2025
Approved by committee 10-DEC-2025
Key points
  • Treats external infusion pumps and associated home infusion drugs as meeting Medicare's durable medical equipment home-use requirement when three criteria are met.
  • Requires that FDA prescribing information say the drug must be given by or under a health professional's supervision, that a qualified home infusion therapy supplier administers or supervises it in the patient's home, and that it is infused at least 12 times per year, either intravenously or subcutaneously or at rates requiring a pump.
  • Takes effect with the first calendar quarter beginning at least one year after enactment.
  • Directs the Secretary of Health and Human Services to ensure patients are notified of their cost sharing for home infusion compared with other infusion settings.
AI-generated from the Introduced in House text of 19-AUG-2025 · verify · report an error
Official CRS summary

Current. The Congressional Research Service's summary covers the bill's latest wording (Introduced in House, 19-AUG-2025).

CRS is the Library of Congress's nonpartisan research office. Read it on congress.gov
Committee referrals (2) Policy area

Health

Sponsor Brian K. Fitzpatrick (R-PA) Cosponsors · 6
■ 4 D■ 2 R