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Itacate Foods LLC Recall: Undeclared Yellow #5 and Yellow #6.

United States

OngoingClass II

Company
Itacate Foods LLC
Product
CHARGE-UP CHILAQUILES Traditional Mexican breakfast consisti…
Recall date
August 20, 2025
Source
FDA

Reason for recall

Undeclared Yellow #5 and Yellow #6.

  1. - Recall initiated
  2. - Reported by source
Recalled products
Product description UPC Quantity Lot / code information
CHARGE-UP CHILAQUILES Traditional Mexican breakfast consisting of tortilla chips smothered in a spicy tomatillo salsa and beans, topped with egg and cheese. NET WT 3.5 OZ (100G) INGREDIENTS: *** VEGETABLE FLAVOR BASE (SALT, SUGAR, SOYBEAN OIL, ONION POWDER, CORN STARCH, MALTODEXTRIN, HYDROLYZED CORN PROTEIN, GARLIC POWDER, TURMERIC (COLOR), SPICES, CARROT JUICE CONCENTRATE, CALCIUM SILICATE (ANTICAKING AGENT), CARAMEL COLOR, NATURAL FLAVORS, DISODIUM INOSINATE, DISODIUM GUANYLATE, CITRIC ACID) *** Not published in this source record 566 packages Lot code: 52061 UPC: 6000877530 Best by date 8/26

Distribution

  • U.S. consignees: AK
  • AZ
  • CA
  • CO
  • GA
  • IL
  • IN
  • LA
  • MA
  • MI
  • MN
  • MT
  • NC
  • NH
  • NJ
  • NM
  • NV
  • NY
  • OR
  • PA
  • SC
  • TX
  • UT
  • VA
  • WA
  • WY

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0648-2025
Event ID
97492
Status
Ongoing
Classification
Class II
Company
Itacate Foods LLC
Product description
CHARGE-UP CHILAQUILES Traditional Mexican breakfast consisting of tortilla chips smothered in a spicy tomatillo salsa and beans, topped with egg and cheese. NET WT 3.5 OZ (100G) INGREDIENTS: *** VEGETABLE FLAVOR BASE (SALT, SUGAR, SOYBEAN OIL, ONION POWDER, CORN STARCH, MALTODEXTRIN, HYDROLYZED CORN PROTEIN, GARLIC POWDER, TURMERIC (COLOR), SPICES, CARROT JUICE CONCENTRATE, CALCIUM SILICATE (ANTICAKING AGENT), CARAMEL COLOR, NATURAL FLAVORS, DISODIUM INOSINATE, DISODIUM GUANYLATE, CITRIC ACID) ***
Quantity
566 packages
Reason
Undeclared Yellow #5 and Yellow #6.
Recall initiation date
August 20, 2025
Report date
September 24, 2025
Classification date
Not published in this source record
Termination date
Not terminated as of this source record
Distribution pattern
U.S. consignees: AK, AZ, CA, CO, GA, IL, IN, LA, MA, MI, MN, MT, NC, NH, NJ, NM, NV, NY, OR, PA, SC, TX, UT, VA, WA, WY
UPC, lot, and code information
Lot code: 52061 UPC: 6000877530 Best by date 8/26
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
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 97492 with 1 other product entry in Public Health Trace.

FDA Recall United States Ongoing Historical recordClass II

Itacate Foods LLC

Product
CAMPSITE LENTEJAS Hearty lentil soup with a tomato and cilan…
Published
September 24, 2025
Distribution
U.S. consignees: AK, AZ, CA, CO, GA, IL,…

View recall →

Responsible company: Itacate Foods LLC

Other recalls from Itacate Foods LLC

FDA Recall United States Ongoing Historical recordClass II

Itacate Foods LLC

Product
CAMPSITE LENTEJAS Hearty lentil soup with a tomato and cilan…
Published
September 24, 2025
Distribution
U.S. consignees: AK, AZ, CA, CO, GA, IL,…

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
Alaska 1
Arizona 1
California 1
Colorado 1
Georgia 1
Illinois 1
Indiana 1
Louisiana 1
Massachusetts 1
Michigan 1
Minnesota 1
Montana 1
North Carolina 1
New Hampshire 1
New Jersey 1
New Mexico 1
Nevada 1
New York 1
Oregon 1
Pennsylvania 1
South Carolina 1
Texas 1
Utah 1
Virginia 1
Washington 1
Wyoming 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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." 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.