Recall record at a glance
| Official record | F-1715-2014 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Roos Foods Inc. |
| Report date | Apr 9, 2014 |
| Recall initiation date | Feb 19, 2014 |
| Quantity | N/A |
| Location | Kenton, DE, United States |
Official product description
Mexicana Cuajadita Casera (Fresh Cheese), 16 oz. wrapped in cellophane on a styrofoam tray, Roos Foods Inc., Kenton, DE 19955 Plant No. 10-5436, UPC code 095548003651. (Ingredients: Cultures, pasteurized milk, salt, natamycin (mold inhibitor)). Santa Rosa de Lima Cuajadita Casera (Fresh Cheese), 16 oz. wrapped in cellophane on a styrofoam tray, Roos Foods Inc., Kenton, DE 19955 Plant No. 10-5436, UPC code 095548003699. (Ingredients: Cultures, pasteurized milk, salt, natamycin (mold inhibitor)). Amigo Brand Cuajadita Casera (Fresh Cheese), 16 oz., wrapped in cellophane on a styrofoam tray, Roos Foods Inc., Kenton, DE 19955 Plant No. 10-5436, UPC code 095548003224. (Ingredients: Cultures, pasteurized milk, salt, natamycin (mold inhibitor)).
Why the product 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, 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
Distribution information
Products were distributed through retail stores in Delaware, Maryland, New Jersey, New York, Virginia and Washington, DC.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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