Herbalife Relaxation Tea Recall: Complete 2025 Update
In July 2025, the Herbalife Relaxation Tea recall became a major topic across health and supplement news platforms. Consumers across the United States, Mexico, and Ecuador were alerted after Herbalife International of America voluntarily recalled nearly 6,000 units of its popular relaxation tea product due to an incorrect ingredient used during manufacturing.
If you purchased this tea recently or are concerned about product safety, this in-depth guide explains everything you need to know including recall details, FDA classification, product identification, possible side effects, and what actions to take.
What Is the Herbalife Relaxation Tea Recall?
On July 21, 2025, Herbalife International of America initiated a voluntary recall of 5,888 units of its Herbalife Nutrition Relaxation Tea.
The reason?
An incorrect ingredient supplied by a third-party vendor was mistakenly used during the manufacturing process.
While the exact identity of the ingredient has not been publicly disclosed, the company acted proactively to remove the affected lot from distribution.
The recall was later classified by the U.S. Food and Drug Administration (FDA) as a Class II recall.
What Does a Class II Recall Mean?
A Class II recall means:
- The product may cause temporary or medically reversible health effects
- The probability of serious adverse health consequences is low
- The risk is not considered life-threatening
This classification is important because it helps consumers understand the severity level.
Why Was Herbalife Relaxation Tea Recalled?
The Herbalife relaxation tea recall was triggered due to a manufacturing error involving an incorrect ingredient.
Key facts:
- The issue originated from a supplier error.
- The incorrect ingredient was incorporated into production.
- The specific ingredient has not been publicly identified.
- No widespread serious injuries were reported at the time of recall.
Because dietary supplements and herbal products rely heavily on ingredient accuracy, even a small deviation can require regulatory action.
Herbalife responded quickly to prevent further distribution.
How to Identify the Recalled Herbalife Relaxation Tea
If you purchased Herbalife tea online, check the packaging carefully. Only one specific lot was affected.
Affected Product Details
- Product Name: Herbalife Nutrition Relaxation Tea
- Net Weight: 1.69 oz (48 g)
- UPC: L044KUS0A-00
- Lot Number: D925507J02
- Expiration Date: April 11, 2027 (04/11/2027)
The affected tea was primarily sold:
- Online nationwide in the United States
- In Mexico
- In Ecuador
If your product does not match these details, it is not part of the recall.
What Ingredients Are Normally in Herbalife Relaxation Tea?
Under normal formulation, Herbalife Relaxation Tea is marketed as a calming herbal blend designed to support:
- Relaxation
- Sleep support
- Stress management
Common botanical ingredients typically include:
- Chamomile
- Lemon balm
- Passionflower
- Lavender
These herbs are widely used in herbal teas for their soothing properties.
However, due to the incorrect ingredient used in the affected lot, the exact composition of the recalled batch may differ from the standard formula.
Potential Side Effects of Herbalife Relaxation Tea
Because the incorrect ingredient was not disclosed, potential side effects specific to the recalled batch remain unclear.
However, typical side effects of herbal relaxation teas may include:
- Mild digestive discomfort
- Drowsiness
- Allergic reactions (rare)
- Interaction with sedatives or blood thinners
If you consumed the recalled product and experienced unusual symptoms, consult a healthcare professional.
What Should Consumers Do?
If you have the affected product:
1. Stop Using It Immediately
Discontinue consumption if the lot number matches.
2. Contact Herbalife Customer Service
Request instructions for returns or refunds.
3. Check Official Recall Information
Review the FDA recall posting for updated details.
Keeping the packaging may help speed up the refund process.
How Serious Is This Recall Compared to Others?
In the supplement industry, recalls can occur due to:
- Undeclared allergens
- Contamination
- Incorrect labeling
- Ingredient substitution
The Herbalife relaxation tea recall falls under ingredient substitution, which is generally considered less severe than contamination or bacterial outbreaks.
Because the FDA classified it as Class II, it indicates the situation is precautionary rather than dangerous.
Is Herbalife a Safe Brand?
Herbalife is a global nutrition company operating in over 90 countries. While the company has faced regulatory scrutiny in the past regarding marketing practices, product recalls like this are not uncommon in the supplement industry.
Importantly:
- The recall was voluntary.
- Only one lot was affected.
- No widespread severe injuries were reported.
Companies that act quickly during recalls often demonstrate stronger quality control systems.
Where Was the Product Sold?
The recalled tea was sold:
- Nationwide in the United States (primarily online)
- Mexico
- Ecuador
Consumers who purchased through independent distributors should also verify lot numbers.
Why Ingredient Accuracy Matters in Herbal Supplements
Dietary supplements are not regulated the same way as prescription drugs. That makes:
- Supplier quality control
- Ingredient testing
- Batch verification
extremely important.
When an incorrect ingredient is introduced, it can:
- Alter effectiveness
- Trigger allergies
- Cause unintended interactions
That is why companies must initiate recalls even when risks appear low.
Impact on Herbalife Customers
The recall raised concerns among:
- Health-conscious consumers
- People using tea for sleep support
- Customers sensitive to ingredient changes
However, since the recall affects a limited batch, most Herbalife tea users are not impacted.
Transparency and communication are critical in maintaining customer trust.
Frequently Asked Questions (FAQ)
1. What is the Herbalife relaxation tea recall about?
The recall involves nearly 6,000 units of Herbalife Nutrition Relaxation Tea due to an incorrect ingredient used during manufacturing.
2. Which lot number is affected?
Lot number D925507J02 with expiration date 04/11/2027.
3. Is the recall dangerous?
The FDA classified it as a Class II recall, meaning temporary or medically reversible health effects are possible, but serious risk is unlikely.
4. What should I do if I bought it?
Stop using the product and contact Herbalife for return or refund instructions.
5. Was all Herbalife tea recalled?
No. Only a specific lot of Herbalife Nutrition Relaxation Tea is affected.
Final Thoughts on the Herbalife Relaxation Tea Recall
The Herbalife relaxation tea recall 2025 highlights the importance of quality control in the dietary supplement industry. While the recall may sound alarming, the FDA classification indicates the risk is relatively low.
If you purchased the product:
- Verify your lot number
- Discontinue use if affected
- Request refund instructions
Most importantly, stay informed through official regulatory updates.
By understanding the details of this recall, you can protect your health while continuing to make confident supplement choices Read More