Queso Fresco Round Cheese (Roos Foods) – Listeria Risk (2014)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Santa Rosa De Lima Queso Fresco Round Fresh Cheese, packaged in 80 oz (5 lbs) cellophane wrapping, Manufacturado por (manufactured for) Roos Foods Inc., Kenton, DE 19955 Plant No. 10-5436,UPC code 095548003569. (Ingredients: Pasteurized whole milk, salt, rennet, calcium, cultures). Santa Rosa de Lima Queso Fresco Round Fresh Cheese, 16 oz. Wrapped in cellophane, Manufacturado por (manufactured for) Roos Foods Inc., Kenton, DE 19955 Plant No. 10-5436,UPC code 095548003569. (Ingredients: Pas
Brand
Roos Foods Inc
Lot Codes / Batch Numbers
all lots and expiration dates, UPC code 095548003569
Products Sold
all lots and expiration dates,UPC code 095548003569
Roos Foods Inc is recalling Santa Rosa De Lima Queso Fresco Round Fresh Cheese, packaged in 80 oz (5 lbs) cellophane wrapping, due to Samples of Santa Rosa De Lima Cuajada en Terron (fresh curd cheese) were found positive for Listeria Monocytogenes. Based on these findings, the firm . This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
DE, IN, MD, NJ, NY, VA, WA, DC
Page updated: Jan 6, 2026