---
title: "Lithium Orotate 2.5; 60 vegetarian capsules, Dietary Supplement; Distributed ... — FDA record H-0447-2025 | Is It on Recall"
description: "Downstream recall of a dietary supplement ingredient that was manufactured out of specifications."
url: https://isitonrecall.com/recall/fda-food-h-0447-2025-lithium-orotate-2-5-60-vegetarian-capsules-dietary-supplement-distributed-by-mecene-llc-447-sutter-s/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# Lithium Orotate 2.5; 60 vegetarian capsules, Dietary Supplement; Distributed by Mecene LLC. 447 Sutter St., Suite 405... — FDA record H-0447-2025

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 24, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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
- **Reason**: Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.
- **Classification**: Class III
- **Recalling firm**: GMP Laboratories of America Inc
- **Quantity**: ~185,482 capsules
- **Agency-reported status**: Terminated
- **Source record identifier**: H-0447-2025

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0447-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 2.5mg Lot #: 21822 Expire date: 09/2026 10mg Lot#: 21108; 22649 Expire date: 10/2025; 01/2028 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)

## Dates in the source

- **Report date**: Aug 20, 2025
- **Recall initiation date**: Jun 24, 2025
- **Center classification date**: Aug 8, 2025
- **Termination date**: Feb 24, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0447-2025%22)

## Related records

[Supplements records](https://isitonrecall.com/product/supplements/) [Supplements records](https://isitonrecall.com/category/supplements/) [GMP Laboratories of America Inc records](https://isitonrecall.com/brand/gmp-laboratories-of-america-inc/)