Wart Remover Recalled

Dercher Enterprises Inc., which does business as Gordon Laboratories, is recalling 5247 jars of Gordofilm wart remover because of deviations from Current Good Manufacturing Practice regulations, according to the May 22, 2024, US Food and Drug Administration (FDA) Enforcement Report. No information on the specific deviations was provided.

The recall affects Gordofilm wart remover (salicylic acid 16.7%), packaged in 15-cc glass jars (NDC 10481-3009-01), from lots F135 (Exp. 3/25), F146 (Exp. 4/25), G103 (Exp. 1/26), and G194 (Exp. 9/26). The product was distributed throughout the United States.

Dercher Enterprises voluntarily initiated the recall on April 12, 2024. On May 13, 2024, the FDA designated the recall Class II. Drugs affected by Class II recalls may cause temporary or medically reversible adverse health consequences if used. While remote, a possibility of serious harm also exists.

Gordofilm is available without a prescription for the treatment of warts and other skin conditions.