RECALL RECORD — CLASS IIIRecall closedF-1360-2013/FDA enforcement

Pina Colada Dessert Bar, 4 OZ

What you need to know

Class III
  • What happened

    Product labeling is incorrect, FD&C colors are undeclared.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDAMI, INMore food

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Product identification

Source: FDA FOOD

Brand namePaleteria Y Neveria La Rosita, LLC
Recalling firmPaleteria Y Neveria La Rosita, LLCSouth Bend, IN, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • firm does not code product
Distribution area
MIIN

Domestic: MI, IN retail stores

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: May 8, 2013
FDA recall numberF-1360-2013

Beyond the headline

The recall, in context

Paleteria Y Neveria La Rosita, LLC initiated this food recall on April 6, 2013. The FDA enforcement report states: Product labeling is incorrect, FD&C colors are undeclared. The FDA report lists distribution as: Domestic: MI, IN retail stores.

The FDA enforcement report describes the reason as: Product labeling is incorrect, FD&C colors are undeclared.

Pina Colada Dessert Bar, 4 OZ was made or distributed by Paleteria Y Neveria La Rosita, LLC in South Bend, IN, United States. This page reflects FDA report F-1360-2013, dated May 8, 2013.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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 lot and date codes 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

Undeclared milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

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 Pina Colada Dessert Bar, 4 OZ recall?

Paleteria Y Neveria La Rosita, LLC recalled Pina Colada Dessert Bar, 4 OZ in an FDA Class III enforcement action reported as F-1360-2013. Product labeling is incorrect, FD&C colors are undeclared.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a milk allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Paleteria Y Neveria La Rosita, LLC 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-1360-2013. 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 Paleteria Y Neveria La Rosita, LLC

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Related alerts

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All alerts

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