Class IIITerminatedVoluntary: Firm initiated
GMP Laboratories of America Inc: food recall H-0447-2025
GMP Laboratories of America Inc of Anaheim, CA recalled Lithium Orotate 2.5; 60 vegetarian capsules, Dietary Supplement; Distributed by Mecene LLC. 447 Sutter St., Suite 405,… Reason: Downstream recall of a dietary supplement ingredient that was manufactured out of specifications. The FDA listed it as Class III in its Enforcement Report dated Aug 20, 2025; distribution: California, Oklahoma.
Record status as published: Terminated (terminated Feb 24, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Lithium Orotate 2.5; 60 vegetarian capsules, Dietary Supplement; Distributed by Mecene LLC. 447 Sutter St., Suite 405, San Fransisco, CA 94108 2.5 mg UPC#: X002T4OPLL 10 mg UPC#: X0031AXVE9
- Product quantity
- ~185,482 capsules
- Reason for recall
- Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.
- Codes, lots and dates on the package
- 2.5mg Lot #: 21822 Expire date: 09/2026 10mg Lot#: 21108; 22649 Expire date: 10/2025; 01/2028
- Distribution pattern
- Distribution was to a single customer who received product in California and Oklahoma.
- Recalling firm
- GMP Laboratories of America Inc, Anaheim, CA
- Classification
- Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jun 24, 2025 |
| Classified by the FDA | Aug 8, 2025 |
| Published in the Enforcement Report | Aug 20, 2025 |
| Terminated | Feb 24, 2026 |
Other products in the same recall event
The FDA groups related products under one recall event (event 97158).
- H-0448-2025 — 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…
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OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0447-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.