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RECALL RECORD — CLASS IRecall closedF-2060-2014/FDA enforcement
Oasis Brands, INC·Food·Jul 31, 2014

Lacteos Santa Martha Quesito Casero Fresh Curd NET Weight 12oz Distributed by Oasis Brands…

What you need to know

Class I

  • What happened

    A State sample came positive for Listeria monocytogenes

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A hardy bacteria that can grow at refrigerator temperatures and cause severe illness in vulnerable groups.

  • Action required

    Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent.

Recall closed · classified by the FDANC, TN, VA, SC +1 moreMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameOasis Brands, INC
Recalling firmOasis Brands, INCMiami, FL, United States
UPC / barcodes
6 35349 00042 0
Lot / date codes
  • UPC 635349 000420 / Exp. Date 092714
Distribution area
NCTNVASCGA

NC (Further shipment by the NC distributors is: TN, VA, NC, SC, and GA).

United States

Quantity affected375 units
Recall initiationFDA report date: September 10, 2014
FDA recall numberF-2060-2014

Beyond the headline

The recall, in context

Oasis Brands, INC initiated this food recall on July 31, 2014. The FDA enforcement report states: A State sample came positive for Listeria monocytogenes. The FDA report lists distribution as: NC (Further shipment by the NC distributors is: TN, VA, NC, SC, and GA).

The FDA enforcement report describes the reason as: A State sample came positive for Listeria monocytogenes

Lacteos Santa Martha Quesito Casero Fresh Curd NET Weight 12oz Distributed by Oasis Brands… was made or distributed by Oasis Brands, INC in Miami, FL, United States. This page reflects FDA report F-2060-2014, dated September 10, 2014.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a hardy bacteria that can grow at refrigerator temperatures and cause severe illness in vulnerable groups.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Listeria monocytogenes

Symptoms to watch for

Fever, muscle aches, nausea and diarrhea may occur. Severe infection can cause headache, stiff neck, confusion, loss of balance or convulsions.

When symptoms may appear

Symptoms can begin within a few days, but can take up to several weeks to appear.

Higher-risk groups

Pregnant people, newborns, adults over 65 and immunocompromised people are at the highest risk of severe illness.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

General guidance based on CDC and FDA consumer information.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Lacteos Santa Martha Quesito Casero Fresh Curd NET Weight 12oz Distributed by Oasis Brands… recall?

Oasis Brands, INC recalled Lacteos Santa Martha Quesito Casero Fresh Curd NET Weight 12oz Distributed by Oasis Brands… in an FDA Class I enforcement action reported as F-2060-2014. A State sample came positive for Listeria monocytogenes

What should I do if I bought this product?

Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Is the Oasis Brands, INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-2060-2014. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Oasis Brands, INC

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Class I·

Oasis Brands, INC

Cuajada En Hoja (Fresh Curd Cheese) in Individually Soft Poly/plastic Bags Labeled in Part: …

Virginia State (VDACS) found Listeria monocytogenes in Lacteos Santa Martha Quesito Casero Fresh Curd (Best by 9/27/14), FDA made an inspection, were the environmental samples…

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Crema Centroamericana (Centroamerican Style Soft Blend Dairy Spread) in Individually Soft…

Virginia State (VDACS) found Listeria monocytogenes in Lacteos Santa Martha Quesito Casero Fresh Curd (Best by 9/27/14), FDA made an inspection, were the environmental samples…

FL, GA, NC +1 moreFood

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.