Backstage Center Recalls Approximately 280 Bottles of Mislabeled Alipotec Raiz de Tejocote
Medical Recalls
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 was exclusively distributed on Amazon.com since September 15, 2023.
Product Name: Alipotec King, Alipotec Raiz de Tejocote
Container 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
There have been no reports of injury or illness, to date.
Consumer Instructions: Consumers should immediately discontinue use of the product. Customers can visit https://alipotecking.com/recall for instructions on how to process the return of the recalled product.
"Backstage Center places the utmost importance on the safety and well-being of our consumers. We deeply regret any worry or inconvenience this recall may have caused. Our commitment to resolving this issue promptly and maintaining the highest standards of product safety and quality remains steadfast. "
Source: FDA
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Consumer Contact: -
Should you require further assistance or have any concerns, please do not hesitate to contact Ben Nissan at 818-452-0005 or via email at info@alipotecking.com.
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Hazard Statement: 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.