Quesito El Establo food recall: Quesito El Establo brand Spanish Cheese QUESITO COLOMBIANO
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 97432
- Recall initiated
- Aug 12, 2025
- Classified by FDA
- Aug 27, 2025
- Posted in Enforcement Report
- Aug 20, 2025
- Terminated
- Mar 12, 2026
- Recalling firm
- Quesito El Establo
- Firm location
- Salem, NH, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Product was manufactured and held under insanitary conditions. Product may be contaminated with Listeria monocytogenes.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Aug 12, 2025. FDA classified it 15 days later, on Aug 27, 2025. Distribution reported by FDA: MA
Recalled products (1)
H-0536-2025 Class I Terminated
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
Codes / lots: All product codes.
Quantity: 800 units
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 97432
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.