Lithium Orotate
Reason Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
Lithium Orotate recall
Recalled by Enjoy Nutrition, LLC; dba Weyland Brain Nutrition · San Francisco, CA, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Lithium Orotate, 1MG, Distributed by Enjoy Nutrition, LLC. UPC#: 717340952714
Quantity: 159,926 units across all product sizes
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot#: 21442; 22647
Where it was sold
Nationwide.
FDA's distribution note: Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Enjoy Nutrition, LLC; dba Weyland Brain Nutrition
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 24, 2025
- In FDA report of
- Aug 20, 2025
- Terminated
- Mar 25, 2026
- FDA recall number
- H-0442-2025 · event 97267
- Official record
- FDA enforcement report search
Also recalled with it (4 more products)
FDA files each product of one recall action separately; these share the same FDA event.
Lithium Orotate
Reason Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
Lithium Orotate
Reason Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
Lithium Orotate
Reason Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.