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RECALL RECORD — CLASS IIRecall closedF-2928-2015/FDA enforcement
Paleteria La Jalpita·Food·May 29, 2015

Rompope (Egg Nog) Bolis (Tube), La Jalpita Brand, 3 FL OZ, No

What you need to know

Class II

  • What happened

    Rompope bolis is recalled due to undeclared Yellow no. 5

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 FDAINMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand namePaleteria La Jalpita
Recalling firmPaleteria La JalpitaPasco, WA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codesNo lot code listed. Follow the recall notice and check the packaging.
Distribution area
IN

distributed in Oregon and Washington

United States

Quantity affected1890 units
Recall initiationFDA report date: August 12, 2015
FDA recall numberF-2928-2015

Beyond the headline

The recall, in context

Paleteria La Jalpita initiated this food recall on May 29, 2015. The FDA enforcement report states: Rompope bolis is recalled due to undeclared Yellow no. 5. The FDA report lists distribution as: distributed in Oregon and Washington.

The FDA enforcement report describes the reason as: Rompope bolis is recalled due to undeclared Yellow no. 5

Rompope (Egg Nog) Bolis (Tube), La Jalpita Brand, 3 FL OZ, No was made or distributed by Paleteria La Jalpita in Pasco, WA, United States. This page reflects FDA report F-2928-2015, dated August 12, 2015.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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 egg

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with an egg 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 egg allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have an egg 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 Rompope (Egg Nog) Bolis (Tube), La Jalpita Brand, 3 FL OZ, No recall?

Paleteria La Jalpita recalled Rompope (Egg Nog) Bolis (Tube), La Jalpita Brand, 3 FL OZ, No in an FDA Class II enforcement action reported as F-2928-2015. Rompope bolis is recalled due to undeclared Yellow no. 5

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 an egg 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 La Jalpita 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-2928-2015. 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 La Jalpita

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