Herbalife Nutrition, Relaxation Tea, Net Wt: 1.69 OZ (48g) UPC# L044KUS0A-00
Summary
The FDA issued a Class II for Herbalife Nutrition, Relaxation Tea, Net Wt: 1.69 OZ (48g) UPC# L044KUS0A-00 by Herbalife International of America. Reason: Incorrect ingredient was received from supplier and used in manufacturing finished product Relaxation Tea..
Details
Source
Food Recall
External ID
H-0390-2025
Action Date
2025-07-30
Status
Terminated
Category
food
Product Description
Herbalife Nutrition, Relaxation Tea, Net Wt: 1.69 OZ (48g) UPC# L044KUS0A-00
Lot/Code Info: Lot# D925507J02 Expiration date: 04/11/2027
Quantity Affected: 5,888 units
Reason for Recall
Incorrect ingredient was received from supplier and used in manufacturing finished product Relaxation Tea.
Distribution
Online sale- US (all state and territories), Mexico and Ecuador
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-21
Company
Los Angeles, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Herbalife International of America has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Herbalife International of America) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Herbalife International of America have FDA actions?
Herbalife International of America has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0390-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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