Recalling firm
GMP Laboratories of America Inc
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-08-20
Distribution
Distribution was to a single customer who received product in California and Oklahoma.
Firm state
CA
Product quantity
~185,482 capsules
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Validation & QualificationReason for recall
Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.
Product description
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
Code / lot info
2.5mg Lot #: 21822 Expire date: 09/2026 10mg Lot#: 21108; 22649 Expire date: 10/2025; 01/2028
Other recalls SPEQ maps to Validation & Qualification
See all Validation & Qualification recalls →Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.