Food Recall Check
Class I · High risk Terminated Initiated Feb 23, 2024 (3 years ago)

Alipotec Raiz de Tejocote dietary supplements recall

Recalled by Backstage Center DBA CTC Seller · Los Angeles, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

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

Quantity: 280 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot Codes: 238124 Expiration date:08-2027

Where it was sold

Nationwide.

FDA's distribution note: Products are distributed to 250 consignees; all consignees were direct to consumer purchases. Distributed nationwide.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Backstage Center DBA CTC Seller
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 23, 2024
In FDA report of
Apr 17, 2024
Terminated
Sep 11, 2024
FDA recall number
F-1147-2024 · event 94118
Official record
FDA enforcement report search

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