RECALL RECORD — CLASS IIIRecall closedF-0768-2020/FDA enforcement
Don Lee Farms·Food·Feb 11, 2020

Chipotle Black Bean Burger 12 Pack/3lbs

What you need to know

Class III
  • What happened

    An ingredient used in the manufacture of finished product was discovered to have been grown using unapproved herbicide.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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 FDACA, IL, WA, MI +2 moreMore food

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Product identification

Source: FDA FOOD

Brand nameDon Lee Farms
Recalling firmDon Lee FarmsMansfield, TX, United States
UPC / barcodes
0 87427 43813 50 87427 43075 7
Lot / date codes
  • Don Lee Farms Item: 997176SF
  • Production lot: 20191220T Don Lee Farms Item: 1372617
  • Production lots: 20191219T, 20200116T, 20200117T, 20200122T, 20200123T
Distribution area
CAILWAMIUTAZ

CA, IL, WA, MI, UT, AZ

United States

Quantity affected4033 cases
Recall initiationFDA report date: February 26, 2020
FDA recall numberF-0768-2020

Beyond the headline

The recall, in context

Don Lee Farms initiated this food recall on February 11, 2020. The FDA enforcement report states: An ingredient used in the manufacture of finished product was discovered to have been grown using unapproved herbicide. The FDA report lists distribution as: CA, IL, WA, MI, UT, AZ.

The FDA enforcement report describes the reason as: An ingredient used in the manufacture of finished product was discovered to have been grown using unapproved herbicide.

Chipotle Black Bean Burger 12 Pack/3lbs was made or distributed by Don Lee Farms in Mansfield, TX, United States. This page reflects FDA report F-0768-2020, dated February 26, 2020.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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

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 Chipotle Black Bean Burger 12 Pack/3lbs recall?

Don Lee Farms recalled Chipotle Black Bean Burger 12 Pack/3lbs in an FDA Class III enforcement action reported as F-0768-2020. An ingredient used in the manufacture of finished product was discovered to have been grown using unapproved herbicide.

What are the symptoms of Product safety recall exposure?

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.

Who is most at risk from Product safety recall?

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

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.

How do I get a refund from Don Lee Farms?

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-0768-2020 and keep the packaging, lot code and proof of purchase if you have them.

Is the Don Lee Farms 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-0768-2020. 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.