PolicyBrief
H.R. 4762
119th CongressJul 25th 2025
Medical Supply Sanctions Act of 2025
IN COMMITTEE

This Act prohibits the export of FDA-approved drugs and prosthetics to the Russian Federation until Russia completely withdraws its military forces from Ukraine.

Morgan Luttrell
R

Morgan Luttrell

Representative

TX-8

LEGISLATION

Mandatory Ban on U.S. Drug and Prosthetic Exports to Russia: What It Means for Global Health Supply Chains

The Medical Supply Sanctions Act of 2025 is a straight-up, no-exceptions mandate: the U.S. must immediately stop exporting specific medical supplies to the Russian Federation. This isn't a suggestion; the bill states the President absolutely must stop these exports, overriding any other existing laws.

The Banned List: FDA-Approved Only

So, what exactly are we talking about? This ban zeroes in on two major categories. First, any "drug" that the FDA has officially approved for sale in the U.S. This covers everything from common prescriptions to specialized cancer treatments, plus every component that goes into them. Second, any "prosthetic device" authorized by the FDA—think artificial limbs, internal joint replacements, or other devices that help a body part work better. Just like with drugs, all parts, accessories, and components for these devices are banned, too. This is not about general medical equipment; it’s specifically about the medications and devices that are essential for long-term health and recovery.

Geopolitical Pressure vs. Patient Access

The goal here is clear: ratchet up the economic pressure on Russia in response to the conflict in Ukraine. For the U.S. government, this is a powerful foreign policy tool. The ban is designed to stay in place until the Secretary of State formally certifies to Congress that Russia has completely ceased its military operations and pulled all forces out of Ukraine. Only then does the export ban automatically lift.

But here’s where the policy meets the pavement. While the intent is to pressure the government, the immediate, tangible impact falls on Russian civilians and patients. If a patient in Russia relies on a specific, patented U.S.-made drug (say, a specialized insulin or a particular cardiac medication) or a high-tech prosthetic component that has no local equivalent, this bill cuts off their supply. For U.S. pharmaceutical and medical device companies, this means an immediate, mandatory loss of a market for specific products, which affects their bottom line and potentially forces them to adjust complex global supply chains.

The Real-World Supply Shock

Imagine a U.S. manufacturer that produces specialized knee replacement components. Even if the Russian customer is a private hospital or an individual patient, this bill mandates that the U.S. company cannot ship that component. This isn't a vague threat; it’s a direct, measurable restriction on trade of essential goods. The clarity in the bill’s language—that the prohibition is absolute and overrides other laws—means there’s very little room for humanitarian exceptions within the scope of the FDA-approved items. While the bill aims to hit the Russian state, the collateral damage involves limiting access to life-sustaining and life-improving medical technology for ordinary people.