Backstage Center DBA CTC Seller Recall: The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.
United States
TerminatedClass I
- Company
- Backstage Center DBA CTC Seller
- Product
- Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35…
- Recall date
- February 23, 2024
- Terminated
- September 11, 2024
- Source
- FDA
Reason for recall
The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled with the "Alipotec King" sticker. Store at room temperature. | Not published in this source record | 280 bottles | Lot Codes: 238124 Expiration date:08-2027 |
Distribution
- Products are distributed to 250 consignees; all consignees were direct to consumer purchases. Distributed nationwide.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1147-2024
- Event ID
- 94118
- Status
- Terminated
- Classification
- Class I
- Company
- Backstage Center DBA CTC Seller
- Product description
- 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
- Reason
- The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.
- Recall initiation date
- February 23, 2024
- Report date
- April 17, 2024
- Classification date
- Not published in this source record
- Termination date
- September 11, 2024
- Distribution pattern
- Products are distributed to 250 consignees; all consignees were direct to consumer purchases. Distributed nationwide.
- UPC, lot, and code information
- Lot Codes: 238124 Expiration date:08-2027
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Backstage Center DBA CTC Seller
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
