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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

Alipotec King Raiz de Tejocote Recalled for Toxic Yellow Oleander Contamination

Agency Publication Date: April 10, 2024
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Summary

Backstage Center (DBA CTC Seller) is recalling 280 bottles of "Alipotec King" Alipotec Raiz de Tejocote dietary supplements because they were found to contain toxic yellow oleander instead of tejocote root. The products were sold in 0.35-ounce plastic bottles and were distributed nationwide through direct-to-consumer sales. No injuries or illnesses have been reported to date, but the manufacturer has initiated this voluntary recall to ensure consumer safety.

Risk

Ingesting yellow oleander can cause severe health complications, including nausea, vomiting, dizziness, diarrhea, heart rhythm irregularities, and potentially death.

What You Should Do

  1. This recall involves Alipotec Raiz de Tejocote dietary supplements (0.35 oz) in plastic bottles labeled with an "Alipotec King" sticker, identified by lot code 238124 and an expiration date of 08-2027.
  2. Contact Backstage Center DBA CTC Seller to arrange for a return, or throw the product away.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 or visit www.fda.gov/safety/recalls for additional information regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact Backstage Center DBA CTC Seller to arrange a return, or contact the supplier for further instructions.
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Alipotec Raiz de Tejocote dietary supplements (0.35 oz)by Alipotec King
Lot Numbers:
238124 (Exp 08-2027)

Plastic bottle labeled with the "Alipotec King" sticker. Store at room temperature.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94118
Status: Resolved
Manufacturer: Backstage Center DBA CTC Seller
Sold By: Direct to consumer purchases
Manufactured In: United States
Units Affected: 280 bottles
Distributed To: Nationwide

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 FDA Press Release 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.