Weyland Brain Nutrition recalls Lithium Orotate 2.5MG products due to failing to meet labeled potency. This downstream recall from supplier affects specific UPCs and lots.
Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
Weyland Brain Nutrition is recalling Lithium Orotate 2.5MG supplements because they don't meet the labeled potency levels. This means the product may not contain the amount of lithium orotate promised on the label, which could affect its intended health benefits.
The product fails to meet the labeled potency, meaning it contains less lithium orotate than advertised. This is a misbranding issue that could lead to the product not providing the intended health benefits. The problem stems from the supplier of the ingredient, not the product itself.
People who purchased Lithium Orotate 2.5MG supplements with the listed UPCs and lots from the manufacturer are affected. Those using the product for health purposes may be at risk of receiving less than the labeled amount of lithium orotate.
Check for the UPC numbers 719318414002 or 709750005289 on the product label. Also look for the lot numbers 21166, 21640, 21821, 22281, or 22757.
Verify the UPC numbers and lot numbers listed in the recall notice to confirm if your product is affected.
The product fails to meet the labeled potency levels, which is a misbranding issue from the supplier of the ingredient.
The recall notice does not specify a remedy, so check the product details to see if it matches the listed UPCs and lots.
No, the recall is for potency issues, not safety hazards like injury or illness.
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-0443-2025 — Weyland Brain Nutrition Weyland Brain Nutrition Hello, I own a Weyland Brain Nutrition that is covered by recall H-0443-2025 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.
