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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

Golean Detox US: Golean DETOX Capsules Recalled for Undeclared Sibutramine and Phenolphthalein

Agency Publication Date: March 13, 2019
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Summary

Golean Detox US is recalling approximately 37 boxes of Golean DETOX capsules because FDA laboratory testing discovered the product contains sibutramine and phenolphthalein. Sibutramine is an appetite suppressant that was removed from the U.S. market in 2010 due to safety concerns regarding heart risks, while phenolphthalein is not approved in the U.S. because of its potential to cause cancer. The product was sold in 28-count boxes containing 14 individual packets and was distributed nationwide. Consumers should stop using this product immediately and contact their healthcare provider or pharmacist for guidance.

Risk

The product contains undeclared sibutramine, which can substantially increase blood pressure and heart rate, posing a significant risk to people with heart disease or high blood pressure. It also contains phenolphthalein, a chemical once used in laxatives that is no longer approved for sale in the U.S. due to concerns that it may cause cancer.

What You Should Do

  1. Check your supplements for Golean DETOX capsules sold in 28-count boxes (14 packets of 2 capsules each) with UPC code 8938510909013.
  2. Verify if you have any lot remaining within its expiration date, as all such lots are included in this recall.
  3. Stop using the product immediately and do not consume any remaining capsules.
  4. Contact your healthcare provider or pharmacist if you have experienced any health problems that may be related to taking this product.
  5. Return any unused product to the place of purchase for a full refund.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Full refund upon return.

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

Affected Products

Product: Golean DETOX capsules (28-count box, 56 g)
UPC Codes:
8938510909013
Lot Numbers:
All lots remaining within expiry

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 82246
Status: Resolved
Manufacturer: Golean Detox US
Sold By: GoLean Detox Enterprise; matxisg.com
Manufactured In: Viet Nam, Malaysia
Units Affected: 37 boxes
Distributed To: Nationwide
Agency Last Updated: March 18, 2019

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 · 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.