Pharmanex Cortitrol

Nu Skin Enterprises INC. recalled Pharmanex Cortitrol in an FDA Class II enforcement action reported as F-1579-2017. Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a soy allergy.

Reactions can begin within minutes to a few hours after eating the product.

People with a diagnosed soy allergy, especially children and anyone with a history of anaphylaxis.

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a soy allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-1579-2017 and keep the packaging, lot code and proof of purchase if you have them.

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

This page is normalized from the openFDA enforcement record F-1579-2017. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.