Weyland Brain Nutrition recalls Lithium Orotate 5MG products with specific UPCs due to potential failure to meet labeled potency. Consumers should check their product details and contact the company for guidance.
Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
Weyland Brain Nutrition is recalling Lithium Orotate 5MG supplements because they may not contain the labeled amount of lithium orotate. This could affect product effectiveness but does not pose a direct health risk.
The product may not contain the labeled amount of lithium orotate, which could lead to inconsistent effectiveness. This is a misbranding issue related to the supplier's product quality, not a direct health hazard.
People who purchased Lithium Orotate 5MG supplements with the listed UPC numbers or lot numbers are affected. Those using the product for medical purposes may be at slightly higher risk due to potential potency issues.
Check for UPC numbers 702730893968 or 702730894064 on the product label. Also look for lot numbers 21123, 21300, 21498, 21783, 21994, 22218, 22299, 22457, 22718, or 23014.
Verify the UPC number and lot number on your Lithium Orotate 5MG supplement to confirm if it is part of the recall.
No, this recall is for potential misbranding and potency issues, not a direct health hazard.
Check for UPC numbers 702730893968 or 702730894064 and lot numbers listed in the recall notice.
The recall does not require immediate action; check your product details and contact Weyland Brain Nutrition for further guidance.
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-0444-2025 — Weyland Brain Nutrition Weyland Brain Nutrition Hello, I own a Weyland Brain Nutrition that is covered by recall H-0444-2025 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.
