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Safety Report: Alipotec King Alipotec Raiz de Tejocote - recalled due toYellow oleander, USA
8 months ago •source fda.gov
Recall notice
United States
Backstage Center is issuing a recall of approximately 280 Bottles of Alipotec Raiz de Tejocote, dietary supplements, that are labeled with the "Alipotec King" sticker. This recall is being initiated because FDA analysis found that the product contains toxic yellow oleander. The product has been exclusively distributed on Amazon.com since September 15, 2023. There have been no reports of injury or illness, to date.The recalled product, which contains yellow oleander instead of tejocote, may induce serious neurologic, gastrointestinal, and cardiovascular adverse health effects. Symptoms may be severe or fatal, including nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac dysrhythmia, and others. Immediate medical attention is advised for consumers experiencing such symptoms.
Product Name: Alipotec King, Alipotec Raiz de TejocoteContainer
Description: Cylindrical bottle with a green top, white body, and contains approximately 30 granules, weighing a total of 0.35oz.
Lot Codes: 238124
Expiration date: 08-2027
Total Distributed: 280 Bottles
Consumer Instructions: Consumers should immediately discontinue use of the product.
In case you experience harm from extraneous materials, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Backstage Center
Brand name: Alipotec King
Product recalled: Alipotec Raiz de Tejocote
Reason of the recall: Product contains yellow oleander, a poisonous plant
FDA Recall date: February 23, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/backstage-center-issuing-recall-approximately-280-bottles-alipotec-raiz-de-tejocote-dietary