Enjoy Nutrition, LLC; dba Weyland Brain Nutrition Recall: Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

🇺🇸 United States

1. June 24, 2025 - Recall initiated
2. August 20, 2025 - Reported by source
3. March 25, 2026 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0444-2025

Event ID

97267

Status

Terminated

Classification

Class III

Company

Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Product description

Lithium Orotate, 5MG, Distributed by Enjoy Nutrition, LLC. UPC#: 702730893968, 702730894064

Quantity

159,926 units across all product sizes

Reason

Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

Recall initiation date

June 24, 2025

Report date

August 20, 2025

Classification date

Not published in this source record

Termination date

March 25, 2026

Distribution pattern

Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide

UPC, lot, and code information

Lot#: 21123; 21300; 21498; 21783; 21994; 22218; 22299; 22457; 22718; 23014

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 97267 with 4 other product entries in Public Health Trace.

Responsible company: Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Other recalls from Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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