Quesito El Establo brand Spanish Cheese QUESITO COLOMBIANO; INGREDIENTS: Milk, Cheese Cultures, Salt, Vitamins C and D;
Summary
The FDA issued a Class I for Quesito El Establo brand Spanish Cheese QUESITO COLOMBIANO; INGREDIENTS: Milk, C by Quesito El Establo. Reason: Product was manufactured and held under insanitary conditions. Product may be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
H-0536-2025
Action Date
2025-08-20
Status
Terminated
Category
food
Product Description
Quesito El Establo brand Spanish Cheese QUESITO COLOMBIANO; INGREDIENTS: Milk, Cheese Cultures, Salt, Vitamins C and D; INGREDIENTES: Leche, Cuajo, Sal, Vitaminas C y D; NET WT. 1 LB.; KEEP REFRIGERATED
Lot/Code Info: All product codes.
Quantity Affected: 800 units
Reason for Recall
Product was manufactured and held under insanitary conditions. Product may be contaminated with Listeria monocytogenes.
Distribution
MA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-08-12
Company
Salem, NH
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 113 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Quesito El Establo) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Quesito El Establo have FDA actions?
This is the only FDA action we have on record for Quesito El Establo in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0536-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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