FDA Recall United States Terminated Historical recordClass II
Herbalife International of America
- Product
- Herbalife NutritionProtein Bar Deluxe - Chocolate Peanut fla…
- Published
- March 23, 2022
- Distribution
- Nationwide
Herbalife International of America Recall: Incorrect ingredient was received from supplier and used in manufacturing finished product Relaxation Tea.
United States
TerminatedClass II
- Company
- Herbalife International of America
- Product
- Herbalife Nutrition, Relaxation Tea, Net Wt: 1.69 OZ (48g) U…
- Recall date
- July 21, 2025
- Terminated
- November 24, 2025
- Source
- FDA
Reason for recall
Incorrect ingredient was received from supplier and used in manufacturing finished product Relaxation Tea.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Herbalife Nutrition, Relaxation Tea, Net Wt: 1.69 OZ (48g) UPC# L044KUS0A-00 | Not published in this source record | 5,888 units | Lot# D925507J02 Expiration date: 04/11/2027 |
Distribution
- Online sale- US (all state and territories)
- Mexico and Ecuador
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0390-2025
- Event ID
- 97291
- Status
- Terminated
- Classification
- Class II
- Company
- Herbalife International of America
- Product description
- Herbalife Nutrition, Relaxation Tea, Net Wt: 1.69 OZ (48g) UPC# L044KUS0A-00
- Quantity
- 5,888 units
- Reason
- Incorrect ingredient was received from supplier and used in manufacturing finished product Relaxation Tea.
- Recall initiation date
- July 21, 2025
- Report date
- July 30, 2025
- Classification date
- Not published in this source record
- Termination date
- November 24, 2025
- Distribution pattern
- Online sale- US (all state and territories), Mexico and Ecuador
- UPC, lot, and code information
- Lot# D925507J02 Expiration date: 04/11/2027
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Herbalife International of America
Other recalls from Herbalife International of America
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:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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.
