Requeson Mexicana Part-Skim Ricotta
Recalling firm: Roos Foods Inc
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,…
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 27, 2015.
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095548003415FDA code information
all lots and expiration dates,UPC code 095548003415
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Full FDA record and distribution details
Original product description
Requeson Mexicana Part-Skim Ricotta, 15 oz., packaged in a plastic cup, Distributed by Roos Foods Inc., Kenton, DE 19955, UPC code 095548003415, (Ingredients: Pasteurized milk, whey, skim milk, cultured milk, solids, carrageenan, salt, potassium sorbate, (preservative)) . Requeson Mexicana Part-Skim Ricotta, 16 oz. packaged in a rigid plastic container (Clamshell), Distributed by Roos Foods Inc., Kenton, DE 19955, UPC code 095548003415, (Ingredients: Pasteurized milk, whey, skim milk, cultured milk, solids, carrageenan, salt, potassium sorbate, (preservative)) .
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 095548003415 | all lots and expiration dates,UPC code 095548003415 |
| UPC | 095548003415 | ed in a plastic cup, Distributed by Roos Foods Inc., Kenton, DE 19955, UPC code 095548003415, (Ingredients: Pasteurized milk, whey, skim milk, cultured milk, solids, carrageenan, salt, potassium sorbate, (preserv |
| UPC | 095548003415 | ntainer (Clamshell), Distributed by Roos Foods Inc., Kenton, DE 19955, UPC code 095548003415, (Ingredients: Pasteurized milk, whey, skim milk, cultured milk, solids, carrageenan, salt, potassium sorbate, (preserv |
Original FDA recall reason
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
Recall details
- Recall number
- F-1706-2014
- Event ID
- 67593
- FDA status
- Terminated
- Initiated
- Feb 19, 2014
- Reported
- Apr 9, 2014
- Classified
- Mar 28, 2014
- Terminated
- Jul 27, 2015
- Quantity
- 122,587-Lbs for all products
- Location
- Kenton, DE, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Visit
Where it was distributed
Products were distributed through retail stores in Delaware, Maryland, New Jersey, New York, Virginia and Washington, DC.
Data updated September 16, 2026. View official FDA data ↗
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