RECALL RECORD — CLASS IIRecall closedF-1250-2023/FDA enforcement

Churritos Corn Flour Sticks, Shelf Stable, 6 Months Shelf Life, Packed in a Rectangular Shape…

What you need to know

Class II
  • What happened

    The product labels include a Contains statement that did not disclose sesame for the product that contains sesame. Sesame is included Ingredient statement.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAIN, OR, CAMore food

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Product identification

Source: FDA FOOD

Brand nameBotanas Michoacanas
Recalling firmBotanas MichoacanasPortland, OR, United States
UPC / barcodes
6 09722 33599 7
Lot / date codes
  • Affected product has BEST BY of 6/01/23 to 12/06/23.
Distribution area
INORCA

Product was distributed in OR and CA.

United States

Quantity affected40 -20 piece cases
Recall initiationFDA report date: July 26, 2023
FDA recall numberF-1250-2023

Beyond the headline

The recall, in context

Botanas Michoacanas initiated this food recall on June 8, 2023. The FDA enforcement report states: The product labels include a Contains statement that did not disclose sesame for the product that contains sesame. Sesame is included Ingredient statement. The FDA report lists distribution as: Product was distributed in OR and CA.

The FDA enforcement report describes the reason as: The product labels include a Contains statement that did not disclose sesame for the product that contains sesame. Sesame is included Ingredient statement.

Churritos Corn Flour Sticks, Shelf Stable, 6 Months Shelf Life, Packed in a Rectangular Shape… was made or distributed by Botanas Michoacanas in Portland, OR, United States. This page reflects FDA report F-1250-2023, dated July 26, 2023.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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 UPC and lot code 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

Undeclared sesame

Symptoms to watch for

Hives, swelling, vomiting, wheezing or anaphylaxis can occur in people with a sesame allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed sesame allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a sesame allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

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 Churritos Corn Flour Sticks, Shelf Stable, 6 Months Shelf Life, Packed in a Rectangular Shape… recall?

Botanas Michoacanas recalled Churritos Corn Flour Sticks, Shelf Stable, 6 Months Shelf Life, Packed in a Rectangular Shape… in an FDA Class II enforcement action reported as F-1250-2023. The product labels include a Contains statement that did not disclose sesame for the product that contains sesame. Sesame is included Ingredient statement.

What are the symptoms of Undeclared sesame exposure?

Hives, swelling, vomiting, wheezing or anaphylaxis can occur in people with a sesame allergy.

How quickly can Undeclared sesame symptoms appear?

Reactions can begin within minutes to a few hours after eating the product.

Who is most at risk from Undeclared sesame?

People with a diagnosed sesame allergy, especially children and anyone with a history of anaphylaxis.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Do not eat the product if you have a sesame allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from Botanas Michoacanas?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-1250-2023 and keep the packaging, lot code and proof of purchase if you have them.

Is the Botanas Michoacanas 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-1250-2023. 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.