Recall record at a glance
| Official record | F-1720-2014 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Roos Foods Inc. |
| Report date | Apr 9, 2014 |
| Recall initiation date | Feb 19, 2014 |
| Quantity | 122,587-Lbs for all products |
| Location | Kenton, DE, United States |
Official product description
Crema Pura Mexicana Brand (Crema Mexicana) Cultured Sour Cream, packaged in a 80 oz Plastic Tub, Grade A, packaged in a 80 oz (5lbs) Plastic Tub, Roos Foods, Inc., Kenton, DE 19955, Plant No. 10-5436, UPC code 095548000247. La Original Crema Pura Mexicana Brand (Crema Mexicana) Cultured Sour Cream , packaged in a 16 oz White Plastic Jar with a yellow plastic lid, Roos Foods, Inc., Kenton, DE 19955, Plant No. 10-5436, UPC code 095548000285. Crema Pura Mexicana Brand (Crema Mexicana) Cultured Sour Cream , Grade A, 30 oz., packed in a plastic jar, Roos Foods, Inc., Kenton, DE 19955, Plant No. 10-5436, UPC code 095548000230. Crema Pura Mexicana Brand (Crema Mexicana) Cultured Sour Cream , Grade A, 16 oz., packed in a plastic pouch, Roos Foods, Inc., Kenton, DE 19955, Plant No. 10-5436, UPC code 095548000407. (Ingredients: Cream, milk, salt, nonfat dry milk, cultured skim milk powder, gelatin, stabilizers (carrageean gum, disodium phosphate), color (annato extract), dairy cultures).
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 II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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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