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RECALL RECORD — CLASS IRecall closedF-1147-2024/FDA enforcement
Backstage Center Dba Ctc Seller·Dietary Supplements·Feb 23, 2024

Alipotec Raiz De Tejocote Dietary Supplements, NET

What you need to know

Class I

  • What happened

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

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDANationwide (US)More supplements

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Product identification

Source: FDA FOOD

Brand nameBackstage Center Dba Ctc Seller
Recalling firmBackstage Center Dba Ctc SellerLos Angeles, CA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot Codes: 238124 Expiration date:08-2027
Distribution area
Nationwide

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

United States

Quantity affected280 bottles
Recall initiationFDA report date: April 17, 2024
FDA recall numberF-1147-2024

Beyond the headline

The recall, in context

Backstage Center Dba Ctc Seller initiated this supplements recall on February 23, 2024. The FDA enforcement report states: The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote. The FDA report lists distribution as: Products are distributed to 250 consignees; all consignees were direct to consumer purchases. Distributed nationwide.

The FDA enforcement report describes the reason as: The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.

Alipotec Raiz De Tejocote Dietary Supplements, NET was made or distributed by Backstage Center Dba Ctc Seller in Los Angeles, CA, United States. This page reflects FDA report F-1147-2024, dated April 17, 2024.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Alipotec Raiz De Tejocote Dietary Supplements, NET recall?

Backstage Center Dba Ctc Seller recalled Alipotec Raiz De Tejocote Dietary Supplements, NET in an FDA Class I enforcement action reported as F-1147-2024. The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Backstage Center Dba Ctc Seller recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1147-2024. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.