Skip to main content
WhoMadeMyFood

FDA recall record

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

Recall F-1147-2024Class ITerminatedFebruary 23, 2024

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of September 11, 2024. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

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

Reason

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

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

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

Code information listed by FDA

Lot Codes: 238124 Expiration date:08-2027

Distribution and firm information

Recalling firm listed by FDA: Backstage Center DBA CTC Seller

Firm location listed by FDA: Los Angeles, CA, United States

Distribution reported by FDA: Products are distributed to 250 consignees; all consignees were direct to consumer purchases. Distributed nationwide.

Product quantity listed by FDA: 280 bottles

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.