CLASS I Food recall · Reported 9 Apr 2014 · FDA Enforcement Report
Santa Rosa de Lima Cuajada en Terron (Fresh Cheese Curd) recalled
Roos Foods is recalling Santa Rosa de Lima Cuajada en Terron (Fresh Cheese Curd), distributed in 7 states. The recall was initiated on 19 Feb 2014 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1718-2014
- FDA event ID
- 67593
- Recalling firm
- Roos Foods, Kenton, DE
- Brand
- Santa Rosa
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 19 Feb 2014
- FDA classified
- 28 Mar 2014
- Reported
- 9 Apr 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Visit
- Reason category
- Listeria
- Product category
- Cheese
Timeline
| 19 Feb 2014 | Recall initiated by company | |
| 28 Mar 2014 | Classified by FDA | +37 days |
| 9 Apr 2014 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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
Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.
Product as listed by the FDA
Santa Rosa de Lima Cuajada en Terron (Fresh Cheese Curd), 16 oz packaged in a plastic bag, Roos Foods Inc., Kenton, DE, 19955, Plant No. 10-5436, UPC code 095548003033. (Ingredients: Pasteurized whole milk, enzymes, rennet & salt). Santa Rosa de Lima Cuajada en Terron, packaged in a 10 lb vacuum packaged plastic bag, Roos Foods Inc., Kenton, DE, 19955, Plant No. 10-5436, UPC code 095548000551. (Ingredients: Pasteurized whole milk, enzymes, rennet & salt). Santa Rosa de Lima Cuajada en Terron Fresh Cheese Curd, 16 oz., packed in a rigid plastic container (Clamshell) Roos Foods Inc., Kenton, DE, 19955, Plant No. 10-5436, UPC code 095548003026. (Ingredients: Pasteurized whole milk, enzymes, rennet & salt).
Where it was distributed
Products were distributed through retail stores in Delaware, Maryland, New Jersey, New York, Virginia and Washington, DC.
District of ColumbiaDelawareMarylandNew JerseyNew YorkVirginiaWashington
Questions about this recall
Is Santa Rosa de Lima Cuajada en Terron (Fresh Cheese Curd) recalled?
Yes. Roos Foods recalled Santa Rosa de Lima Cuajada en Terron (Fresh Cheese Curd) on 19 Feb 2014. The recall is Class I and its status is Terminated. Recall number F-1718-2014.
Why was it 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
Which lots are affected?
all lots and expiration dates, UPC code 095548003033, UPC code 095548000551, UPC code 095548003026
Where was it sold?
Products were distributed through retail stores in Delaware, Maryland, New Jersey, New York, Virginia and Washington, DC.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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|---|---|---|---|---|---|
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