Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported April 17, 2024
Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled with the "Alipotec King" sticker. Store at room temperature.
The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.
Backstage Center DBA Ctc Seller recalled Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled wi… - a critical-severity action.
Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled wi… was recalled by Backstage Center DBA Ctc Seller in April 17, 2024. Reason: The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of t…. Check the official notice for the remedy. Verify recall #F-1147-2024 with the FDA Food before acting.
The recall
Backstage Center DBA Ctc Seller issued this critical-severity FDA Food recall-The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of t….
- Critical
- severity level
- Class I
- classification
- April 17, 2024
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1147-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1147-2024) was formally reported on April 17, 2024, with the manufacturer initiating the action on February 23, 2024. It is classified under Critical severity (Class I), with a current status of Terminated. Backstage Center DBA Ctc Seller is listed as the recalling firm, operating out of Los Angeles, CA. Federal records list the affected scope as 280 bottles.
The documented reason for this recall is: The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote. Distribution data in the federal record shows the product reached: Products are distributed to 250 consignees; all consignees were direct to consumer purchases. Distributed nationwide.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
280 bottles
Related Recalls
6
0 from same agency
Product description
Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled with the "Alipotec King" sticker. Store at room temperature.
Reason for recall
The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1147-2024 |
| Date reported | April 17, 2024 |
| Date initiated | February 23, 2024 |
| Recalling firm | Backstage Center DBA Ctc Seller |
| Firm location | Los Angeles, CA |
| Affected scope | 280 bottles |
| Distribution | Products are distributed to 250 consignees; all consignees were direct to consumer purchases. Distributed nationwide. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1147-2024) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled with the "Alipotec King" sticker. Store at room temperature.. Recalled by Backstage Center DBA Ctc Seller. Units affected: 280 bottles.
Why was this product recalled? ▼
The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on April 17, 2024. Severity: Critical. Recall number: F-1147-2024.
Where was the recalled product distributed? ▼
Distribution: Products are distributed to 250 consignees; all consignees were direct to consumer purchases. Distributed nationwide..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1147-2024) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported April 17, 2024. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.