Class ITerminated in FDA datasetRecall initiated Feb 23, 2024

Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled with the…

Recalling firm: Backstage Center DBA CTC Seller

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 11, 2024.

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ProductAlipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled with the "Alipotec King" sticker. Store at room temperature.
Package size0.35oz

FDA code information

Lot Codes: 238124 Expiration date:08-2027

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
lot238124Lot Codes: 238124 Expiration date:08-2027

Original FDA recall reason

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

Recall details

Recall number
F-1147-2024
Event ID
94118
FDA status
Terminated
Initiated
Feb 23, 2024
Reported
Apr 17, 2024
Classified
Apr 10, 2024
Terminated
Sep 11, 2024
Quantity
280 bottles
Location
Los Angeles, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Products are distributed to 250 consignees; all consignees were direct to consumer purchases. Distributed nationwide.

FDA source record · F-1147-2024

Data updated September 16, 2026. View official FDA data ↗

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