Food recall

Herbalife International of America recall: Herbalife Nutrition, Relaxation Tea

Herbalife International of America, of Los Angeles, CA, recalled Herbalife Nutrition, Relaxation Tea. The FDA's reason: “Incorrect ingredient was received from supplier and used in manufacturing finished product Relaxation Tea.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on July 21, 2025, and the FDA first listed it in its Enforcement Report of July 30, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Labeling, packaging or manufacturing problems

Status

Terminated

Closed November 24, 2025

The recall

Company
Herbalife International of America (Los Angeles, CA)
Reason, in FDA's words
“Incorrect ingredient was received from supplier and used in manufacturing finished product Relaxation Tea.”
Where it was sold
Online sale- US (all state and territories), Mexico and Ecuador
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
97291

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0390-2025 Class II

    Herbalife Nutrition, Relaxation Tea, Net Wt: 1.69 OZ (48g) UPC# L044KUS0A-00

    Codes: Lot# D925507J02 Expiration date: 04/11/2027

    Quantity: 5,888 units

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of July 30, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.