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RECALL RECORD — CLASS IRecall closedF-1662-2014/FDA enforcement
Pecan Shed·Food·Jan 10, 2014

Pumpkin Pie Fudge

What you need to know

Class I

  • What happened

    Presence of undeclared allergens soy, and milk

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. Tree nuts such as almonds or walnuts were not declared, posing a risk to people with tree-nut allergy.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDAIN, ID, TX, OR +7 moreMore food

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Product identification

Source: FDA FOOD

Brand namePecan Shed
Recalling firmPecan ShedWichita Falls, TX, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • product has no lot codes or expiration dates. Per firm, fudge expires in 2 weeks unless frozen. If frozen, it expires in 2 years
Distribution area
INIDTXORMNDCMTPAIAAZGA

Product is sold at onsite retail store and through the internet (5%) to customers in ID, TX, OR, MN, Washington DC, MT, PA, IA, AZ, GA

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: March 19, 2014
FDA recall numberF-1662-2014

Beyond the headline

The recall, in context

Pecan Shed initiated this food recall on January 10, 2014. The FDA enforcement report states: Presence of undeclared allergens soy, and milk. The FDA report lists distribution as: Product is sold at onsite retail store and through the internet (5%) to customers in ID, TX, OR, MN, Washington DC, MT, PA, IA, AZ, GA.

The FDA enforcement report describes the reason as: Presence of undeclared allergens soy, and milk

Pumpkin Pie Fudge was made or distributed by Pecan Shed in Wichita Falls, TX, United States. This page reflects FDA report F-1662-2014, dated March 19, 2014.

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, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

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

Undeclared tree nuts

Symptoms to watch for

Hives, swelling, wheezing, digestive symptoms or anaphylaxis can occur in people with a tree-nut 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 tree-nut allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a tree-nut 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 Pumpkin Pie Fudge recall?

Pecan Shed recalled Pumpkin Pie Fudge in an FDA Class I enforcement action reported as F-1662-2014. Presence of undeclared allergens soy, and milk

What are the symptoms of Undeclared tree nuts exposure?

Hives, swelling, wheezing, digestive symptoms or anaphylaxis can occur in people with a tree-nut allergy.

How quickly can Undeclared tree nuts symptoms appear?

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

Who is most at risk from Undeclared tree nuts?

People with a diagnosed tree-nut allergy, especially children and anyone with a history of anaphylaxis.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a tree-nut 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 Pecan Shed?

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-1662-2014 and keep the packaging, lot code and proof of purchase if you have them.

Is the Pecan Shed 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-1662-2014. 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

Brand history

More recalls by Pecan Shed

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Class I·

Pecan Shed

Chocolate Mint Fudge

Presence of undeclared allergens soy, and milk

IN, ID, TX +8 moreFood
Class II·

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Candied Pecans: Creamy White

Presence of undeclared soy allergen

IN, ID, TX +8 moreFood

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