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RECALL RECORD — CLASS IIRecall closedF-1784-2015/FDA enforcement
Fiesta Pacific Products INC.·Food·Feb 25, 2015

Horchata Post Mix Fountain Syrup, 3 Gallons (11.4 Liters)

What you need to know

Class II

  • What happened

    Fiesta Pacific is recalling all Brown Label Horchata due a formulation error and no process on file to prevent the growth of potentially harmful bacteria, including Clostridium…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Clostridium botulinum can produce a severe neurotoxin in improperly processed or stored food.

  • 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 FDACA, NV, UT, CO +1 moreMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameFiesta Pacific Products INC.
Recalling firmFiesta Pacific Products INC.San Diego, CA, United States
UPC / barcodes
0 09319 00006 0
Lot / date codes
  • Batch No. EA410406 EA410506 EA411306 EA411906 EA412406 EA412606 EA410307 EA410807 EA411007 EA412407 EA412807 EA410608 EA410708 EA412008 EA412208 EA410309 EA410909 EA411809 EA412309 EA410210 EA410210 EA410910 EA411610 EA411710 EA412010 EA412110 EA412210 EA410511 EA411311 EA411411 EA411811 EA412011 EA412411 EA412711 EA410112 EA411512 EA411512 EA411612 EA411812 EA412212 EA412312 EA412312 EA510501 EA510501 EA510601 EA510801 EA511601 EA512301 EA512601 EA510202 EA510302 EA510402
Distribution area
CANVUTCOAZ

CA, NV, UT, CO, AZ

United States

Quantity affected13, 386 units
Recall initiationFDA report date: April 8, 2015
FDA recall numberF-1784-2015

Beyond the headline

The recall, in context

Fiesta Pacific Products INC. initiated this food recall on February 25, 2015. The FDA enforcement report states: Fiesta Pacific is recalling all Brown Label Horchata due a formulation error and no process on file to prevent the growth of potentially harmful bacteria, including Clostridium botulinum. The FDA report lists distribution as: CA, NV, UT, CO, AZ.

The FDA enforcement report describes the reason as: Fiesta Pacific is recalling all Brown Label Horchata due a formulation error and no process on file to prevent the growth of potentially harmful bacteria, including Clostridium botulinum.

Horchata Post Mix Fountain Syrup, 3 Gallons (11.4 Liters) was made or distributed by Fiesta Pacific Products INC. in San Diego, CA, United States. This page reflects FDA report F-1784-2015, dated April 8, 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, clostridium botulinum can produce a severe neurotoxin in improperly processed or stored food.

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 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

Botulism

Symptoms to watch for

Possible blurred or double vision, drooping eyelids, slurred speech, difficulty swallowing, muscle weakness and breathing difficulty. Seek urgent medical care for these symptoms.

When symptoms may appear

Neurological symptoms typically begin 12 to 36 hours after exposure, but can appear sooner or later.

Higher-risk groups

Infants, older adults, pregnant people and people with weakened immune systems are especially vulnerable.

What to do now

  1. 1Do not taste, eat or use the affected product, even if it looks or smells normal.
  2. 2Seek urgent medical care immediately if anyone has neurological or breathing symptoms; do not wait for test results.
  3. 3Keep the product packaging and contact the recalling firm or retailer about a refund or safe disposal.

Botulism is a medical emergency. Contact emergency services for breathing or neurological symptoms.

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 Horchata Post Mix Fountain Syrup, 3 Gallons (11.4 Liters) recall?

Fiesta Pacific Products INC. recalled Horchata Post Mix Fountain Syrup, 3 Gallons (11.4 Liters) in an FDA Class II enforcement action reported as F-1784-2015. Fiesta Pacific is recalling all Brown Label Horchata due a formulation error and no process on file to prevent the growth of potentially harmful bacteria, including Clostridium…

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. Do not taste, eat or use the affected product, even if it looks or smells normal. Seek urgent medical care immediately if anyone has neurological or breathing symptoms; do not wait for test results. Keep the product packaging and contact the recalling firm or retailer about a refund or safe disposal.

Is the Fiesta Pacific Products 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-1784-2015. 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

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