Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Lithium Orotate 2.5 Recalled by GMP Laboratories of America Inc Due to Downstream recall of a dietary supplement ingredient that...

Date: June 24, 2025
Company: GMP Laboratories of America Inc
Status: Terminated
Source: FDA (Food)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact GMP Laboratories of America Inc directly.

Affected Products

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

Quantity: ~185,482 capsules

Why Was This Recalled?

Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.

Where Was This Sold?

Distribution was to a single customer who received product in California and Oklahoma.

About GMP Laboratories of America Inc

GMP Laboratories of America Inc has 3 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Food). Last updated March 26, 2026. View original report