Check the Batch
Class ITerminated in FDA datasetRecall initiated Feb 19, 2014

Mexicana Brand Queso Fresco Fresh Cheese

Recalling firm: Roos Foods Inc

Why it was recalled

Samples of Santa Rosa De Lima Cuajada en Terron (fresh curd cheese) were found positive for Listeria Monocytogenes. Based on these findings, the firm recalled all brands, lots,…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 27, 2015.

Check your package

Compare the exact product and package details with the label you have.

ProductMexicana Brand Queso Fresco Fresh Cheese, 16 oz. Wrapped in cellophane, ) Roos Foods, Inc., Kenton, DE 19955, Plant No. 10-5436, UPC code 095548003330 (Ingredients: Cultured and pasteurized milk, salt).
Package size16 oz
UPC095548003330

FDA code information

all lots and expiration dates, UPC code 095548003330

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Mexicana Brand Queso Fresco Fresh Cheese, 16 oz. Wrapped in cellophane, ) Roos Foods, Inc., Kenton, DE 19955, Plant No. 10-5436, UPC code 095548003330 (Ingredients: Cultured and pasteurized milk, salt).

Extracted codes and context

TypeCode / valueContext
UPC095548003330all lots and expiration dates, UPC code 095548003330
UPC095548003330n cellophane, ) Roos Foods, Inc., Kenton, DE 19955, Plant No. 10-5436, UPC code 095548003330 (Ingredients: Cultured and pasteurized milk, salt).

Original FDA recall reason

Samples of Santa Rosa De Lima Cuajada en Terron (fresh curd cheese) were found positive for Listeria Monocytogenes. Based on these findings, the firm recalled all brands, lots, date codes, and container sizes of the cheese products that were manufactured and/or repackaged in their facility. Out of an abundance of caution, the firm expanded the recall to include all brands, lots, date codes, and c

Recall details

Recall number
F-1712-2014
Event ID
67593
FDA status
Terminated
Initiated
Feb 19, 2014
Reported
Apr 9, 2014
Classified
Mar 28, 2014
Terminated
Jul 27, 2015
Quantity
122,587-Lbs for all products
Location
Kenton, DE, United States
Initiation type
Voluntary: Firm initiated
Notification
Visit

Where it was distributed

Products were distributed through retail stores in Delaware, Maryland, New Jersey, New York, Virginia and Washington, DC.

FDA source record · F-1712-2014

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.