← FDA ENFORCEMENT
F-1147-2024Class I

Backstage Center DBA CTC Seller

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Backstage Center DBA CTC Seller
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2024-04-17
Distribution
Products are distributed to 250 consignees; all consignees were direct to consumer purchases. Distributed nationwide.
Firm state
CA
Product quantity
280 bottles
Initiated by
Voluntary: Firm initiated
Reason for recall

The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.

Product description

Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled with the "Alipotec King" sticker. Store at room temperature.

Code / lot info

Lot Codes: 238124 Expiration date:08-2027

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →