Food Recall Check
Class III · Low risk Terminated Initiated Jun 24, 2025 (16 months ago)

Lithium Orotate 2.5 recall

Recalled by GMP Laboratories of America Inc · Anaheim, CA, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

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

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

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

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

2.5mg Lot #: 21822 Expire date: 09/2026 10mg Lot#: 21108; 22649 Expire date: 10/2025; 01/2028

Where it was sold

California Oklahoma

FDA's distribution note: Distribution was to a single customer who received product in California and Oklahoma.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
GMP Laboratories of America Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 24, 2025
In FDA report of
Aug 20, 2025
Terminated
Feb 24, 2026
FDA recall number
H-0447-2025 · event 97158
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

Class III · Low risk Terminated Other

Lithium Orotate Weyland Brain Nutrition

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

GMP Laboratories of America Inc CA, OK H-0448-2025

Other recalls by GMP Laboratories of America Inc

Class II · Moderate risk Terminated Other

Dietary supplement Product is labeled as

Reason The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.

GMP Laboratories of America Inc Nationwide F-2297-2012

Recent dietary supplements recalls

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