Lithium Orotate — Class III food recall H-0448-2025
Terminated recall by GMP Laboratories of America Inc, reported 2025-08-20, distributed in CA, OK. Downstream recall of a dietary supplement ingredient that was manufactured out of specification.
| Recall number | H-0448-2025 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GMP Laboratories of America Inc, Anaheim, CA, United States |
| Recall initiated | 2025-06-24 |
| Classified | 2025-08-08 |
| Reported by FDA | 2025-08-20 |
| Terminated | 2026-02-24 |
| Distributed | CA, OK |
| Quantity | 185,482 capsules |
| Reason classes | specification failure |
| Lot numbers | 1000MCG, 21107, 21123, 21166, 21181, 21288, 21300, 21301, 21371, 21442, 21498, 21499, 21505, 21640, 21695, 21783, 21821, 21911, 21993, 21994, 22105, 22106, 22200, 22218, 22257, 22281, 22299, 22397, 22399, 22457, 22556, 22557, 22647, 22650, 22718, 22736, 22757, 22918 |
Product
Lithium Orotate, Weyland Brain Nutrition ; 60 vegetarian capsules, Dietary Supplement; Distributed by Enjoy Nutirtion, LLC. San Francisco, CA 94108, (415) 894-0537 2.5 mg UPC#: X001SBI13J 5 mg UPC#: X000PY16Z5 10 mg UPC#: X000T9B9B7 20 mg UPC#: X001VBLW8H 1000 MCG UPC#: X003SBV661
Reason for recall
Downstream recall of a dietary supplement ingredient that was manufactured out of specification.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/H-0448-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.