Skip to main content
Medium RiskFDAfda-H-0446-2025MISLABELED

Lithium Orotate, 20MG, Distributed by Enjoy Nutrition, LLC. UPC#: none

Category
Units Affected
159,926
Recall Date
June 24, 2025
Issuing Agency
Hazard
Mislabeled

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0446-2025.

Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0446-2025.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Enjoy Nutrition, Llc; Dba Weyland Brain Nutrition or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0446-2025.

Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Enjoy Nutrition, Llc; Dba Weyland Brain Nutrition Recall FAQ

Enjoy Nutrition, Llc; Dba Weyland Brain Nutrition is the subject of a food safety report: Lithium Orotate, 20MG, Distributed by Enjoy Nutrition, LLC. UPC#: none. The notice was published on June 24, 2025 by the U.S. Food and Drug Administration (FDA). Approximately 159,926 units are potentially affected.