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RECALL RECORD — CLASS IIRecall closedF-0118-2013/FDA enforcement
Sunshine Peanut Company·Food·Feb 17, 2012

Product Is 50 lb Bag Peanut Butter

What you need to know

Class II

  • What happened

    On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling…

  • 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, NJ +1 moreMore food

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Product identification

Source: FDA FOOD

Brand nameSunshine Peanut Company
Recalling firmSunshine Peanut CompanyJacksonville, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • lot code: 113112.
Distribution area
INCAFLNJWA

Product was distributed to distributors in CA, FL, NJ, and WA.

United States

Quantity affected48 boxes (10/5 Lb Bags) & 225 boxes (50 Lb Bags)
Recall initiationFDA report date: October 24, 2012
FDA recall numberF-0118-2013

Beyond the headline

The recall, in context

Sunshine Peanut Company initiated this food recall on February 17, 2012. The FDA enforcement report states: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling by USDA found the products to contain Aflatoxin levels greater than 20 ppb. The FDA report lists distribution as: Product was distributed to distributors in CA, FL, NJ, and WA.

The FDA enforcement report describes the reason as: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling by USDA found the products to contain Aflatoxin levels greater than 20 ppb.

Product Is 50 lb Bag Peanut Butter was made or distributed by Sunshine Peanut Company in Jacksonville, FL, United States. This page reflects FDA report F-0118-2013, dated October 24, 2012.

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 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 peanut

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a peanut 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 peanut allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a peanut 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 Product Is 50 lb Bag Peanut Butter recall?

Sunshine Peanut Company recalled Product Is 50 lb Bag Peanut Butter in an FDA Class II enforcement action reported as F-0118-2013. On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling…

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 peanut 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.

Is the Sunshine Peanut Company 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-0118-2013. 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 Sunshine Peanut Company

View brand
Class II·

Sunshine Peanut Company

Sunny Boy Peanut Butter

On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling…

IN, CA, FL +2 moreFood
Class II·

Sunshine Peanut Company

Product Is 1 OZ Peanut Butter

On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling…

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