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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 Food
Food & Beverages/Dietary Supplements

Tapee Tea Recalled for Undeclared Dexamethasone and Piroxicam

Agency Publication Date: January 19, 2024
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Summary

THE WIEDEMANN COMPANY LLC is recalling 3,600 packs of Tapee Tea because laboratory samples confirmed the presence of dexamethasone and piroxicam, which are not listed on the packaging. These are potent drug ingredients that should only be used under medical supervision. No incidents or injuries have been reported in connection with this recall. Consumers should stop using the tea immediately and return it for a refund or dispose of it.

Risk

Dexamethasone is a corticosteroid and piroxicam is a non-steroidal anti-inflammatory drug (NSAID); consuming these undeclared drugs without medical supervision can lead to serious health complications or dangerous interactions with other medications.

What You Should Do

  1. This recall affects Tapee Tea packaged in paper packets containing 5 packets per bag, identified by Lot No. 40-2-00658-2-0012 and a Best By date of 10/08/2025.
  2. Return the product to the place of purchase for a refund, throw it away, or contact THE WIEDEMANN COMPANY LLC for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Tapee Tea (5 packets per bag)
Lot Numbers:
40-2-00658-2-0012 (Best By 10/08/2025)

Recall Number F-0775-2024; 3,600 packs affected.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93413
Status: Resolved
Manufacturer: THE WIEDEMANN COMPANY LLC
Sold By: Retailers in OH and FL
Manufactured In: United States
Units Affected: 3600 packs
Distributed To: Ohio, Florida

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.