FDA Enforcement Actions Related to
Homeopathic or Alleged Homeopathic Products

Stephen Barrett, M.D.

Warning Letters (57)

Nearly all of these ordered the seller to stop claiming that products could effectively treat specific diseases of conditions. Some ordered the seller to stop claiming that products were vaccine equivalents. A few involved failure to use good manufacturing practices (GMP).

Product Recalls (3)

Recalls are generally voluntary actions taken after the FDA notifies the company that a product poses an unacceptable risk.

This article was revised on January 1, 2018.

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