CLASS II Food recall · Reported 30 Jul 2025 · FDA Enforcement Report
Herbalife Nutrition, Relaxation Tea recalled
Herbalife International of America is recalling Herbalife Nutrition, Relaxation Tea. The recall was initiated on 21 Jul 2025 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0390-2025
- FDA event ID
- 97291
- Recalling firm
- Herbalife International of America, Los Angeles, CA
- Brand
- Herbalife Nutrition
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 21 Jul 2025
- FDA classified
- 6 Aug 2025
- Reported
- 30 Jul 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Labeling Errors
- Product category
- Herbal Supplements
Timeline
| 21 Jul 2025 | Recall initiated by company | |
| 30 Jul 2025 | Published in enforcement report | +9 days |
| 6 Aug 2025 | Classified by FDA | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Incorrect ingredient was received from supplier and used in manufacturing finished product Relaxation Tea.
Product as listed by the FDA
Herbalife Nutrition, Relaxation Tea, Net Wt: 1.69 OZ (48g) UPC# L044KUS0A-00
Where it was distributed
Online sale- US (all state and territories), Mexico and Ecuador
Questions about this recall
Why was it recalled?
Incorrect ingredient was received from supplier and used in manufacturing finished product Relaxation Tea.
Which lots are affected?
Lot# D925507J02 Expiration date: 04/11/2027
Where was it sold?
Online sale- US (all state and territories), Mexico and Ecuador
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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