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Class IIITerminated in FDA datasetRecall initiated Feb 11, 2020

Don Lee Farms Chipotle Black Bean Burger 12 pack/3Lbs. cartons

Recalling firm: Don Lee Farms

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 7, 2020.

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Compare the exact product and package details with the label you have.

ProductDon Lee Farms Chipotle Black Bean Burger 12 pack/3Lbs. cartons UPC 087427438135, Item 1372617 Don Lee Farms Chipotle Black Burger 10 pack/2.5 lb. cartons UPC 087427430757/Item 997176SF
Package size3Lbs
UPC087427430757, 087427438135

FDA code information

Don Lee Farms Item: 997176SF; Production lot: 20191220T Don Lee Farms Item: 1372617; Production lots: 20191219T, 20200116T, 20200117T, 20200122T, 20200123T

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Don Lee Farms Chipotle Black Bean Burger 12 pack/3Lbs. cartons UPC 087427438135, Item 1372617 Don Lee Farms Chipotle Black Burger 10 pack/2.5 lb. cartons UPC 087427430757/Item 997176SF

Extracted codes and context

TypeCode / valueContext
UPC087427430757Item 1372617 Don Lee Farms Chipotle Black Burger 10 pack/2.5 lb. cartons UPC 087427430757/Item 997176SF
UPC087427438135Don Lee Farms Chipotle Black Bean Burger 12 pack/3Lbs. cartons UPC 087427438135, Item 1372617 Don Lee Farms Chipotle Black Burger 10 pack/2.5 lb. cartons UPC 087427430757/Item 997176SF
lot20191220TDon Lee Farms Item: 997176SF; Production lot: 20191220T Don Lee Farms Item: 1372617; Production lots: 20191219T, 20200116T, 20200117T, 20200122T, 20200123T

Original FDA recall reason

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

Recall details

Recall number
F-0768-2020
Event ID
84956
FDA status
Terminated
Initiated
Feb 11, 2020
Reported
Feb 26, 2020
Classified
Mar 3, 2020
Terminated
Apr 7, 2020
Quantity
4033 cases
Location
Mansfield, TX, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

CA, IL, WA, MI, UT, AZ

FDA source record · F-0768-2020

Data updated September 16, 2026. View official FDA data ↗

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