FDA Food recall ·
Lithium Orotate 2.5 recall
- Recall number
- H-0447-2025
- Date
- (initiated June 24, 2025)
- Company / brand
- GMP Laboratories of America Inc
2931 E La Jolla St, Anaheim, CA, United States - Category
- Food › Class III
- Classification
- Class III
- Status
- Terminated
- Units affected
- ~185,482 capsules
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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
Why was it recalled?
Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
2.5mg Lot #: 21822 Expire date: 09/2026 10mg Lot#: 21108; 22649 Expire date: 10/2025; 01/2028
Distribution
Distribution was to a single customer who received product in California and Oklahoma.
States: California Oklahoma
What does Class III mean?
Class III means use of or exposure to the product is not likely to cause adverse health consequences (for example, a labeling violation).
Source: FDA (food), recall H-0447-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.