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RECALL RECORD — CLASS IIRecall closedF-0700-2021/FDA enforcement
John B. Sanfilippo & Son INC.·Food·May 28, 2021

Favorite Day Monster Trail Mix, Product Number 04313

What you need to know

Class II

  • What happened

    Trail Mixes may contain stringy pieces of flexible plastic

  • 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 FDANationwide (US)More food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameJohn B. Sanfilippo & Son INC.
Recalling firmJohn B. Sanfilippo & Son INC.Elgin, IL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot 1067GY0A Best By 08/MAR/2022 GY
Distribution area
Nationwide

Nationwide

United States

Quantity affected12, 017 cases (8 items per case)
Recall initiationFDA report date: June 30, 2021
FDA recall numberF-0700-2021

Beyond the headline

The recall, in context

John B. Sanfilippo & Son INC. initiated this food recall on May 28, 2021. The FDA enforcement report states: Trail Mixes may contain stringy pieces of flexible plastic. The FDA report lists distribution as: Nationwide.

The FDA enforcement report describes the reason as: Trail Mixes may contain stringy pieces of flexible plastic

Favorite Day Monster Trail Mix, Product Number 04313 was made or distributed by John B. Sanfilippo & Son INC. in Elgin, IL, United States. This page reflects FDA report F-0700-2021, dated June 30, 2021.

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

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 Favorite Day Monster Trail Mix, Product Number 04313 recall?

John B. Sanfilippo & Son INC. recalled Favorite Day Monster Trail Mix, Product Number 04313 in an FDA Class II enforcement action reported as F-0700-2021. Trail Mixes may contain stringy pieces of flexible plastic

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. 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 John B. Sanfilippo & Son 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-0700-2021. 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 John B. Sanfilippo & Son INC.

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Class I·

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