GMP Laboratories is recalling Lithium Orotate 2.5 dietary supplements that were manufactured out of specifications. Consumers should check product labels for UPC codes X002T4OPLL or X0031AXVE9 and lot numbers 21822 or 21108/22649.
Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.
GMP Laboratories is recalling Lithium Orotate 2.5 dietary supplements because they were made outside the required quality standards. This recall is a downstream effect of a manufacturing issue that could affect product safety.
The supplements were manufactured out of specifications, meaning they did not meet the required quality standards. This could potentially lead to inconsistent product performance or safety issues, though the exact risk level is not specified in the recall.
People who purchased Lithium Orotate 2.5 dietary supplements with UPC codes X002T4OPLL or X0031AXVE9 and lot numbers 21822, 21108, or 22649 are affected. Those who use dietary supplements for health reasons may be at slightly higher risk.
Check the product label for UPC codes X002T4OPLL (2.5mg) or X0031AXVE9 (10mg). Also look for lot numbers 21822 (2.5mg), 21108 or 22649 (10mg).
Look for UPC codes X002T4OPLL or X0031AXVE9 and lot numbers 21822, 21108, or 22649 on the supplement packaging.
The recall states the product was manufactured out of specifications, but the official notice does not specify if it is safe to use.
The recall does not provide specific action steps for consumers, only product identification details.
Check the product label for UPC codes X002T4OPLL or X0031AXVE9 and lot numbers 21822, 21108, or 22649.
We’ve drafted a message you can send GMP Laboratories to request your refund or repair — edit it as you like.
Subject: Recall H-0447-2025 — GMP Laboratories GMP Laboratories Hello, I own a GMP Laboratories that is covered by recall H-0447-2025 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.
