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Marty Makary Resigns as FDA Commissioner Amid Policy Disputes

2026-05-13

The BareStory

Dr. Marty Makary resigned as commissioner of the Food and Drug Administration on Tuesday after serving for more than a year. The president announced the resignation on social media and appointed Kyle Diamantas, a deputy commissioner for food policy, to serve as acting commissioner. The president also publicly shared a text message from Makary highlighting his work on drug approval processes.

Makary’s departure followed reported disagreements between the commissioner and the administration. According to a senior administration official and sources familiar with the matter, tensions involved the slow implementation of policies, including the approval of flavored e-cigarettes. Furthermore, anti-abortion organizations had recently demanded Makary’s removal, accusing him of delaying a safety review of the abortion medication mifepristone that was requested by Health and Human Services Secretary Robert F. Kennedy Jr.

The resignation concludes a tenure marked by internal agency challenges. Senior FDA officials accused Makary of micromanagement, a lack of transparency, and mishandling a fast-track drug voucher program. The agency has recently experienced leadership turmoil, including the departure of several career scientists and reports of declining staff morale.

Makary, a surgeon who had previously criticized the government’s response to the COVID-19 pandemic, was confirmed to lead the FDA in March 2025. Following his departure, a scheduled Senate subcommittee hearing was postponed. As acting commissioner, Diamantas will inherit the ongoing mifepristone review and upcoming regulatory negotiations with the pharmaceutical industry.

Left Perspective

  • Shielding Reproductive Civil Liberties
  • Defending Independent Scientific Accountability
  • Blocking Corporate Safety Shortcuts

Right Perspective

  • Enforcing Executive Policy Mandates
  • Prioritizing Traditional Social Order
  • Restoring Institutional Management Discipline

How it may affect me

As a U.S. reader:

• Short-term access to the abortion medication mifepristone may be affected as the new acting commissioner takes over an ongoing safety review prioritized by the administration.

• Consumers might soon see faster regulatory decisions or market availability for flavored e-cigarettes, as the agency aims to eliminate previous implementation delays.

• The speed and safety of new medications entering the market could change over the long term, depending on how new leadership manages the fast-track drug voucher program and upcoming negotiations with the pharmaceutical industry.

• The recent departure of career FDA scientists and internal morale issues could lead to long-term shifts in how rigorously the agency conducts independent safety reviews for food and drugs.

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