GMP Laboratories recalls Lithium Orotate dietary supplements manufactured out of specification. Consumers should check product labels for UPC codes and expiration dates to determine if affected.
Downstream recall of a dietary supplement ingredient that was manufactured out of specification.
GMP Laboratories is recalling Lithium Orotate supplements because they were made outside quality standards. This could pose a risk to consumers using these supplements.
The supplements were manufactured out of specification, meaning they do not meet quality standards. This could lead to potential health risks if consumed, though the exact nature of the risk is not specified in the recall.
People who purchased Lithium Orotate supplements from Enjoy Nutrition, including those with specific UPC codes and expiration dates listed in the recall notice. Those with the product in their possession are most at risk.
Check for the product name 'Lithium Orotate, Weyland Brain Nutrition' on the label. Look for UPC codes: X001SBI13J (2.5mg), X000PY16Z5 (5mg), X000T9B9B7 (10mg), X001VBLW8H (20mg), X003SBV661 (1000 MCG). Also check the expiration dates listed in the recall notice.
Look for the product name 'Lithium Orotate, Weyland Brain Nutrition' and the specific UPC codes listed in the recall notice.
The product was manufactured out of specification, meaning it does not meet quality standards.
Check for the product name 'Lithium Orotate, Weyland Brain Nutrition' and the specific UPC codes listed in the recall notice.
The recall notice does not specify a remedy, so consumers should check with the manufacturer or distributor for further instructions.
We’ve drafted a message you can send GMP Laboratories to request your refund or repair — edit it as you like.
Subject: Recall H-0448-2025 — GMP Laboratories GMP Laboratories Hello, I own a GMP Laboratories that is covered by recall H-0448-2025 from GMP Laboratories. 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.
