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Lithium Orotate 2.5

Recalled — do not eat Announced August 20, 2025 - Closed - Class III

Lithium Orotate 2.5 from GMP Laboratories of America Inc was recalled on August 20, 2025. Reason for the recall: Downstream recall of a dietary supplement ingredient that was manufactured out of specifications. It was sold in California, Oklahoma. Identify it by lot 21822 Expire date: 09/2026 10mg Lot#: 21108. As of the latest federal update, the FDA classification is Class III and the recall status is terminated. Do not consume - Check details.

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Recalled products

ProductLot / codeClassRecall #
Lithium Orotate 2.521822 Expire date: 09/2026 10mg Lot#: 21108Class IIIH-0447-2025
Lithium Orotate, Weyland Brain Nutrition21166, 21640, 21821, 22281, 22757 Expire date: 11/2025, 09…Class IIIH-0448-2025

Where it was sold

States named in the notice: California, Oklahoma.

Timeline

Announced (first public date)
August 20, 2025
Recall started by the firm
June 24, 2025
Classified by the FDA
August 8, 2025
Terminated
February 24, 2026

Official source: FDA recall notice

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