# FDA recall F-1720-2014

> **Roos Foods Inc** · Class II · food recall initiated 2014-02-19.

## Product

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).

## Reason for recall

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

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

## Key facts

- **Recall number:** F-1720-2014
- **Recalling firm:** Roos Foods Inc
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2014-02-19
- **Report date:** 2014-04-09
- **Termination date:** 2015-07-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kenton, DE, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-1720-2014

## Citation

> AI Analytics. FDA recall F-1720-2014. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/F-1720-2014. Source: US FDA. Licensed CC0.

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