Weyland Brain Nutrition recalls Lithium Orotate 1MG (UPC 717340952714) due to failing to meet labeled potency. This downstream recall from a supplier affects products sold with specific lot numbers.
Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
Weyland Brain Nutrition is recalling Lithium Orotate 1MG supplements because they don't meet the labeled potency levels. This means the product may not provide the intended nutritional benefits as advertised.
The product fails to meet the labeled potency, meaning it contains less lithium orotate than advertised. This could result in the supplement not providing the intended nutritional benefits. The issue is a downstream recall from the supplier of the ingredient, not a direct safety hazard.
People who purchased Lithium Orotate 1MG supplements with UPC 717340952714 and lot numbers 21442 or 22647 are affected. Those using the product for nutritional purposes are most at risk of receiving less than the labeled amount of lithium orotate.
Check for the UPC code 717340952714 and lot numbers 21442 or 22647 on the product label. The product is sold under the brand Weyland Brain Nutrition.
Look for the UPC code 717340952714 and lot numbers 21442 or 22647 on the supplement packaging.
The product fails to meet the labeled potency levels, meaning it contains less lithium orotate than advertised. This is a downstream recall from the supplier of the ingredient.
The official recall notice does not specify a remedy or action for affected products.
The recall is for potency failure, not a safety hazard. There is no risk of injury or serious health effects.
We’ve drafted a message you can send Weyland Brain Nutrition to request your refund or repair — edit it as you like.
Subject: Recall H-0442-2025 — Weyland Brain Nutrition Weyland Brain Nutrition Hello, I own a Weyland Brain Nutrition that is covered by recall H-0442-2025 from Weyland Brain Nutrition. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
