Product Wiki · Recalls · U.S. FDA — Food Enforcement

Recall H-0447-2025 — 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

U.S. FDA — Food Enforcement · United States · 2025-06-24 · Class III

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Food Enforcement
Recall identifier
H-0447-2025
Date of alert
2025-06-24
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
GMP Laboratories of America Inc
Product category
food
Product type
Food
Reported risk: Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.