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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Qikmoov LLC: Vy&Tea Recalled Due to Presence of Unlisted Drug Sibutramine

Agency Publication Date: July 30, 2021
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Summary

Qikmoov LLC is recalling 591 boxes of Vy&Tea, a Vietnamese herbal weight loss tea, because FDA laboratory analysis found the product contains sibutramine. Sibutramine is a controlled substance that was removed from the U.S. market in 2010 for safety reasons and is not listed on the product label. The affected tea is sold in boxes containing 15 sachets (45.0G) and features Vietnamese labeling with a green leaf and bird logo. Consumers who have purchased this product should stop using it immediately and contact their healthcare provider.

Risk

Sibutramine can significantly increase blood pressure and heart rate in some people, posing a serious risk to those with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. This hidden drug ingredient may also interact in life-threatening ways with other medications a consumer might be taking.

What You Should Do

  1. Identify the affected product by looking for Vy&Tea boxes labeled with a green leaf and a bird underneath, containing 15 tea sachets (45.0G).
  2. Check the packaging for a 'Best By' date of 9/2021 to confirm if your product is part of the recall.
  3. Stop using the Vy&Tea product immediately and dispose of any remaining sachets.
  4. Contact your healthcare provider or pharmacist for guidance, especially if you have experienced any side effects while using this product.
  5. Return any unused product to the place of purchase for a refund and contact Qikmoov LLC for further instructions.
  6. For additional questions or to report a related health issue, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Contact healthcare provider and return for refund.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Vy&Tea (Vietnamese Labeling) (15 tea sachets per box, 45.0G)
Model:
D-0749-2021
Date Ranges: Best By Date: 9/2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 88280
Status: Active
Manufacturer: Qikmoov LLC
Sold By: the internet
Manufactured In: United States, Vietnam
Units Affected: 591 boxes
Distributed To: Nationwide
Agency Last Updated: August 17, 2021

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.