CHARGE-UP CHILAQUILES Traditional Mexican breakfast consisting of…
Reason Undeclared Yellow #5 and Yellow #6.
CAMPSITE LENTEJAS Hearty lentil soup with a tomato and cilantro… recall
Recalled by Itacate Foods LLC · Sacramento, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared Yellow #5 and Yellow #6.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
CAMPSITE LENTEJAS Hearty lentil soup with a tomato and cilantro base that takes no time to rehydrate. NET WT 4.0 OZ (115G) 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: 154 packages
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot: 52060 UPC: 6000877531 Best by date 8/27
Where it was sold
Alaska Arizona California Colorado Georgia Illinois Indiana Louisiana Massachusetts Michigan Minnesota Montana North Carolina New Hampshire New Jersey New Mexico Nevada New York Oregon Pennsylvania South Carolina Texas Utah Virginia Washington Wyoming
FDA's distribution note: 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
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away.
- Recalling firm
- Itacate Foods LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 20, 2025
- In FDA report of
- Sep 24, 2025
- FDA recall number
- H-0649-2025 · event 97492
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.