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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Food

Queseria Bendita: Panela soft cheese is recalled because of a potential to be contaminated with Listeria monocytogenes.; Queso Fresco soft cheese is recalled because of a potential to be contaminated with Listeria monocytogenes.; Requeson soft cheese is recalled because of a potential to be contaminated with Listeria monocytogenes.; Cotija cheese is recalled because of a potential to be contaminated with Listeria monocytogenes.; Sour Cream/Crema Agria is recalled because of a potential to be con

Agency Publication Date: February 26, 2015
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Affected Products

Product: Panela, Latin Style Soft Cheese, packaged in plastic wrap, Net Wt. 1 lb. The UPC is 6 10074 99341 4

all lot, all best by dates up to 041615

Product: Queso Fresco, Latin Style Soft Cheese, packaged in plastic wrap, Net Wt. 1 lb. or 3 lbs. The UPC of 1 lb. package is 0 94922 10602 5. There is NO UPC for 3 lbs. package.

all lot, all best by dates up to 041615

Product: Requeson, Latin Style Soft Cheese, packaged in a plastic tub, Net Wt. 1 lb. The UPC is 0 94922 10603 2.

all lot, all best by dates up to 041615

Product: Cotija cheese is packaged in a plastic wrap, Net Wt. 1 lb. There is no UPC

None

Product: Sour Cream/Crema Agria is packaged in a plastic tub, Net Wt. 1 lb. The UPC is 0 94922 10608 7.

None

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 70296
Status: Resolved
Manufacturer: Queseria Bendita
Manufactured In: United States
Units Affected: 5 products (undetermined because firm does not keep record; undetermined because firm does not keep record; undetermined because firm does not keep record; undetermined because firm does not keep record; undetermined because firm does not keep record)

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.