Food FDA Class II Ongoing Mislabeling
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, CARR
Itacate Foods LLC Published Sep 24, 2025
Risk level
Class IIMay cause a temporary or reversible health problem; slight chance of serious harm.
Severity score 67/100
What should you do?
- Check whether you have this product, using the lot codes, UPCs, and dates listed below.
- Do not eat, serve, or sell the affected product.
- Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
- Contact Itacate Foods LLC or your place of purchase with questions, and see the source record below for full details.
Reason for recall
Undeclared Yellow #5 and Yellow #6.
Affected products (1)
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) ***
154 packages
UPC: 6000877531
Lot codes: 52060
Code info: Lot: 52060 UPC: 6000877531 Best by date 8/27
Affected areas
AlaskaArizonaCaliforniaColoradoGeorgiaIllinoisIndianaLouisianaMassachusettsMichiganMinnesotaMontanaNevadaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaOregonPennsylvaniaSouth CarolinaTexasUtahVirginiaWashingtonWyoming
Timeline
- InitiatedAug 20, 2025
- PublishedSep 24, 2025
- Recall number
- H-0649-2025
- Agency
- U.S. Food and Drug Administration
- Country
- US
FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.