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Green Chile Foods, Inc. Recall: Green Chile Concepts, LLC is voluntarily recalling certain Green Chile Food Company brand burritos sold frozen, refrigerated and/or served hot in certain convenience stores, vending machines, and retail locations because they may have the potential to be contaminated with Listeria monocytogenes.

United States

TerminatedClass I

Company
Green Chile Foods, Inc.
Product
Bean & Cheese Burrito with Monterey Jack, Salsa, Green Chile…
Recall date
May 13, 2017
Terminated
July 5, 2017
Source
FDA

Reason for recall

Green Chile Concepts, LLC is voluntarily recalling certain Green Chile Food Company brand burritos sold frozen, refrigerated and/or served hot in certain convenience stores, vending machines, and retail locations because they may have the potential to be contaminated with Listeria monocytogenes.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Bean & Cheese Burrito with Monterey Jack, Salsa, Green Chile, Rice, & Serrano Peppers!, Item # 484, Case UPC 8 33425 00086 3, Item UPC 8 83350 02411 3. Unit Size 8oz. Packaged in Paper Wrap sealed with Item Label, 12 units per case. Frozen or refrigerated. Not published in this source record 5168 cs Case Lot Code: 17079, 17090, 17107,17112

Distribution

  • Artic Cascade and DOT Foods. No VA/govt/military or foreign consignees.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2253-2017
Event ID
77302
Status
Terminated
Classification
Class I
Company
Green Chile Foods, Inc.
Product description
Bean & Cheese Burrito with Monterey Jack, Salsa, Green Chile, Rice, & Serrano Peppers!, Item # 484, Case UPC 8 33425 00086 3, Item UPC 8 83350 02411 3. Unit Size 8oz. Packaged in Paper Wrap sealed with Item Label, 12 units per case. Frozen or refrigerated.
Quantity
5168 cs
Reason
Green Chile Concepts, LLC is voluntarily recalling certain Green Chile Food Company brand burritos sold frozen, refrigerated and/or served hot in certain convenience stores, vending machines, and retail locations because they may have the potential to be contaminated with Listeria monocytogenes.
Recall initiation date
May 13, 2017
Report date
June 7, 2017
Classification date
Not published in this source record
Termination date
July 5, 2017
Distribution pattern
Artic Cascade and DOT Foods. No VA/govt/military or foreign consignees.
UPC, lot, and code information
Case Lot Code: 17079, 17090, 17107,17112
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 77302 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

Green Chile Foods, Inc.

Product
Bean & Cheddar with Salsa, FIRE ROASTED Corn & Red Bell Pepp…
Published
June 7, 2017
Distribution
Artic Cascade and DOT Foods. No VA/govt…

View recall →

Responsible company: Green Chile Foods, Inc.

Other recalls from Green Chile Foods, Inc.

FDA Recall United States Terminated Historical recordClass I

Green Chile Foods, Inc.

Product
Bean & Cheddar with Salsa, FIRE ROASTED Corn & Red Bell Pepp…
Published
June 7, 2017
Distribution
Artic Cascade and DOT Foods. No VA/govt…

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Virginia 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.