Lithium orotate 2.5 mg product recalled for failing labeled potency specification
Lithium Orotate 2.5 mg distributed by Enjoy Nutrition, LLC is recalled nationwide because it does not meet its labeled potency. The action follows a recall by the ingredient supplier.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The rubric puts FDA Class III actions at 1 or 2, and this is a potency and labeling shortfall with no health hazard described in the notice.
Plain-English summary
Lithium Orotate, 2.5 mg, distributed by Enjoy Nutrition, LLC, is being recalled. The affected product carries UPC 719318414002 and 709750005289, and lot numbers 21166, 21640, 21821, 22281 and 22757. The recall covers 159,926 units across all product sizes, distributed nationwide, including through Amazon, Excel 3PL and Encore Fulfillment.
The recall was issued for under potency and misbranding: the product fails to meet its labeled lithium orotate potency. It is a downstream recall arising from a recall by the supplier of the ingredient. The FDA classified the action as Class III.
Customers should check the UPC and lot number on the package against the list above. Recalled product should not be used and can be returned to the seller.
The recalled product
- Product
- Lithium Orotate, 2.5MG, Distributed by Enjoy Nutrition, LLC. UPC#: 719318414002; 709750005289
- Manufacturer
- Enjoy Nutrition, LLC; dba Weyland Brain Nutrition
- Category
- Food — Dietary Supplement
- Hazard
- subpotency
- misbranding
- downstream-recall
- class-iii
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (5)
- Lot#: 21166
- 21640
- 21821
- 22281
- 22757
Distribution
Distributed nationwide across the United States.
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