Herbalife Relaxation Tea Recall: Safety Risks And Future Course

Today’s topic: Herbalife Relaxation Tea Recall

The recall of Herbalife Relaxation Tea, initiated in July 2025 by Herbalife International of America, sparked widespread concern in the consumer market. Close to 6,000 packages of this highly popular drink were recalled from distribution.

Herbalife accounted for this recall because this product contains an “incorrect ingredient received from supplier and used in manufacturing”. This can pose health risks to consumers in three countries.

Here’s what you need to know about the Herbalife Relaxation Tea Recall.

• Product Identification: Which lots are being recalled and how to check your canister.
• The Risk Factor: The importance of FDA classifying this recall as ‘Class II’.
• The Supply Chain Gap: How a mistaken ingredient passed into the finished product.
• Customer Action: What you must do if you possess a recalled container, including how to submit reports of side effects.

What Prompted The Herbalife Relaxation Tea Recall

The situation began when a major error in their supply chain was spotted in this company. The Herbalife Relaxation Tea Recall has led a lot of this product being recalled from the market.

Description Of Recalled Product

Herbalife International of America announced the immediate voluntary recall of 5,888 packages of Herbalife Nutrition Relaxation Tea. Consumers of the product must take immediate action to see if their product information matches these identifying factors:

• Product: Herbalife Nutrition Relaxation Tea
• UPC: L044KUS0A-00
• Lot Number: D925507J02
• Expiration Date: 04/11/2027

The product was sold online in all states in the US. Other countries where this product was delivered include Mexico and Ecuador, apart from others. Because of the global nature of this product, this product is very difficult to track down.

The Problem was that an ingredient used was out of place.

The notice of recall, filed with the U.S. Food & Drug Administration (FDA), further elucidates this problem: “Incorrect ingredient received from supplier and used in manufacturing finished product Relaxation Tea”.

Although Herbalife refused to disclose which exact ingredient they had used in error, it remains suspicious in consumers’ minds which hazard they were exposing them to.

Such an error immediately identifies a problem with Good Manufacturing Practices at the company. Herbalife fails to test each of its herbal ingredients in a blend before mixing them to make the final product.

Defining The Risk: FDA Class II Recall

On August 6, 2025, the FDA labeled the Herbalife Relaxation Tea Recall a class II risk. Of course, you need to grasp an understanding of this designation. A class II designation is serious. 

This is because it affects a case in which a patient gets exposure to an adverse product, which can lead to an inability of a temporarily reversible ill health effect (FDA). Furthermore, a serious ill health consequence remains a remote possibility.

The categorization shows that the health hazard posed by this unknown ingredient can come in moderate symptoms, which may not threaten lives but can be equally uncomfortable.

Such symptoms may include everything from gastrointestinal problems and allergic reactions to temporary pain and interaction with prescription drugs. Therefore, this makes the Herbalife Relaxation Tea Recall all the more urgent.

What To Do If You Have A Teabag Containing Recalled Tea?

If you have Herbalife Relaxation Tea in your kitchen, you need to check your lot numbers immediately. You should avoid drinking them if your numbers correspond with the lots in the recall.

1. Codes

Check the Codes. Your packaging should be from the lot number D925507J02 and the expiration date should be 04/11/2027.

2. Stop Use

Of course, if the numbers match, stop using the tea immediately. Do not give it to any other person, especially a loved one, like children or senior citizens.

3. Contacting Herbalife

Contact Herbalife’s customer service. They will instruct you on what to do and the procedure of returning the product to them for a refund or replacement.

4. Dispose Safely

Dispose of it according to Herbalife’s instructions. But if you really must discard it, you may put it in a sealed bag to prevent other people from using it.

What Should You Do If You Have Already Drunk The Tea?

As the Herbalife Relaxation Tea Recall contains an unknown ingredient, consumers who consumed this product have to be very observant of their bodies.

Observation Of Symptoms

Remediate the symptoms if you notice any of the listed unusual reactions that include nausea, vomiting, an allergic reaction such as rashes or swelling, headache, and insomnia.

Medical Consultation

If you experience any of the side effects from consumption of this herbal tea, you must consult your physician immediately. Inform your physician about the Herbalife Relaxation Tea Recall and other unidentified ingredients.

Report The Reaction

You play an essential role in consumer protection. To report an adverse reaction, go to the FDA MedWatch Safety Reporting Portal. This information allows FDA monitoring of the severity of the problem and informs FDA decisions related to the issuance of a higher class recall, such as a class I recall.

Behind The Scenes: The Supply Chain Failure

The Herbalife Relaxation Tea Recall epitomizes the major flaws in the dietary supplement industry. A product like herbal tea would possess a huge and complex global supply chain.

The Challenge Of Ingredient Sourcing

Herbalife’s Relaxation Tea includes ingredients like lemon balm, passionflower, lavender, and chamomile herbs. Herbal products often originate from foreign suppliers in their raw form.

An ingredient may be incorrectly labeled, adulterated, or substituted at any point from the time of harvesting to processing and packaging.

Here, the lack of oversight allowed a mistaken ingredient to slip through quality control. Such a situation can occur when a manufacturer is provided a wrongly labeled source ingredient from a supplier.

Such a situation can also occur when an organization does not conduct tests to identify an arriving source.

Loopholes In The Regulation Of Dietary Supplements

Herbal teas and other dietary supplements fall under a different rule than prescription drugs do. The FDA does not regulate dietary supplements prior to public consumption.

The safety and labeling of a dietary supplement are primarily treated as the responsibility of the manufacturer, according to the FDA.

A regulation brought into place mainly by the DSHEA of 1994 relies primarily upon companies like Herbalife to adhere to strict GMP guidelines.

Herbalife Relaxation Tea Recall took place because of a simple combination mistake in an ingredient. This shows how companies have utterly failed in fulfilling their most basic role of upholding control over their environments.

Role Of Online Sales

The fact that the Herbalife product is being sold online increases the difficulty of the recall procedure.

This issue of direct consumption sales hinging on the acceptance of the recall notice by various distributors and shoppers makes it easier to accomplish a product recall by merely removing items from store shelves.

The Herbalife Relaxation Tea Recall is yet another case illustrating how companies approach recalls when attempting to quickly pull off the market a product made available to consumers around the globe online.

Read Also: Joy Luck Dried Lily Flowers Recall – Check Your Pantry Now

Best Practices for Safe Tea & Supplement Use

Consumers must learn a lesson from Herbalife Relaxation Tea Recall. Taking proactive measures will help you limit your risk if you purchase supplements or herbal teas.

Selecting Trustworthy Products Search For Third Party Certification

Select brands which manufacture products under the certification of third parties. Certification from such bodies as USP or NSF will make sure a product has undergone voluntary tests for the purity, name, and strength of an ingredient.

Demand Transparency

Support companies that are transparent with all their product ingredients and sources. Brands with complete lab analysis are a good indication.

Consult Your Doctor

We should always run any new health drink/supplement by our healthcare expert. Check if you have any sort of pre-existing medical condition, ask them to check if this supplement or health drink will interact with the prescription drugs. 

For special cases of pregnancy or nursing, one should stay extra careful. 

General Safety Practices

Checking the Packaging, always. It is imperative to check the lot number, UPC code, and expiration dates of all supplements and food items before consumption.

Reporting Problems With A Product

If a product looks suspicious, either by smell or some kind of reaction, do not continue to take it and report it to the FDA immediately.

Global Reach: Cross-Border Herbalife Relaxation Tea Recall

The international scope of the Herbalife Relaxation Tea Recall complicates things in this case. Herbalife sold this product internationally through online sales to consumers in 

• the United States,
• Mexico,
• and Ecuador.

Diverse Landscapes Of Regulation

The recall procedure must work in cooperation with not two but rather three different regulatory regimes. Evaluation for risk by the FDA is done in relation to consumers in the United States. Health authorities should also see to it that in Mexico and Ecuador, this product ceases to circulate in markets.

Recall In Mexico and Ecuador?

The Herbalife Relaxation Tea Recall is international in scope. Such products are distributed online in the US, as well as in Mexico and Ecuador. 

Frequently Asked Questions (FAQs):

The Class II recall points to a serious situation but is not as time-sensitive as a recall for a life-threatening situation in a Class I recall. 

A product with a Class II recall can cause a consumer to get a temporarily reversible medical consequence. You can submit reports of any side effects or product complaints to the FDA MedWatch Safety Reporting Portal. Alternatively, you can direct complaints to your state’s health department.