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RECALL RECORD — CLASS IIRecall closedF-0666-2019/FDA enforcement
Thatchers Gourmet Specialties INC.·Food·Nov 13, 2018

Gingerbread Popcorn

What you need to know

Class II

  • What happened

    Ingredient statement lists flour but does not declare wheat as a sub-ingredient.

  • 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, CA, FL, SC +1 moreMore food

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Product identification

Source: FDA FOOD

Brand nameThatchers Gourmet Specialties INC.
Recalling firmThatchers Gourmet Specialties INC.San Francisco, CA, United States
UPC / barcodes
4 00020 87356 90 05182 99523 50 05182 99522 5
Lot / date codes
  • Lot number/expiration date DU0518261524 4/8/2019
  • DU0518264525 4/12/2019
  • D00518299523 5/10/2019
  • D00518299522 5/10/2019.
Distribution area
INCAFLSCHI

Disney locations in CA, FL, SC, HI No foreign distribution.

United States

Quantity affected2898 units
Recall initiationFDA report date: December 5, 2018
FDA recall numberF-0666-2019

Beyond the headline

The recall, in context

Thatchers Gourmet Specialties INC. initiated this food recall on November 13, 2018. The FDA enforcement report states: Ingredient statement lists flour but does not declare wheat as a sub-ingredient. The FDA report lists distribution as: Disney locations in CA, FL, SC, HI No foreign distribution.

The FDA enforcement report describes the reason as: Ingredient statement lists flour but does not declare wheat as a sub-ingredient.

Gingerbread Popcorn was made or distributed by Thatchers Gourmet Specialties INC. in San Francisco, CA, United States. This page reflects FDA report F-0666-2019, dated December 5, 2018.

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 wheat or gluten

Symptoms to watch for

Wheat allergy can cause hives, nausea, cramps, breathing difficulty or anaphylaxis. For celiac disease, even small amounts of gluten can cause intestinal damage.

When symptoms may appear

Allergic reactions can begin within minutes to hours. Celiac-related intestinal effects may be delayed.

Higher-risk groups

People with wheat allergy, celiac disease, non-celiac gluten sensitivity or a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a wheat allergy or must avoid gluten.
  2. 2Seek emergency care for breathing difficulty or other signs of a severe allergic reaction.
  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 Gingerbread Popcorn recall?

Thatchers Gourmet Specialties INC. recalled Gingerbread Popcorn in an FDA Class II enforcement action reported as F-0666-2019. Ingredient statement lists flour but does not declare wheat as a sub-ingredient.

What are the symptoms of Undeclared wheat or gluten exposure?

Wheat allergy can cause hives, nausea, cramps, breathing difficulty or anaphylaxis. For celiac disease, even small amounts of gluten can cause intestinal damage.

How quickly can Undeclared wheat or gluten symptoms appear?

Allergic reactions can begin within minutes to hours. Celiac-related intestinal effects may be delayed.

Who is most at risk from Undeclared wheat or gluten?

People with wheat allergy, celiac disease, non-celiac gluten sensitivity or 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 wheat allergy or must avoid gluten. Seek emergency care for breathing difficulty or other signs of a severe allergic reaction. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from Thatchers Gourmet Specialties INC.?

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-0666-2019 and keep the packaging, lot code and proof of purchase if you have them.

Is the Thatchers Gourmet Specialties INC. 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-0666-2019. 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.