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Horchata Post Mix Fountain Syrup, 3 gallons (11.4 Liters), UPC 0 09319 00006 0.

FDA Recall #F-1784-2015 — Class II — February 25, 2015

Recall Summary

Recall NumberF-1784-2015
Date InitiatedFebruary 25, 2015
ClassificationClass II
StatusTerminated
TypeVoluntary: Firm initiated
Product TypeFood

Recalling Firm

FirmFiesta Pacific Products Inc.
LocationSan Diego, CA

Product Description

Horchata Post Mix Fountain Syrup, 3 gallons (11.4 Liters), UPC 0 09319 00006 0.

Reason for Recall

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.

Classification

Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

Distribution Pattern

CA, NV, UT, CO, AZ

Product Quantity

13,386 units

Product Codes / Lot Numbers

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

What Should You Do?

Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.

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Frequently Asked Questions

Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.

In most cases, yes. Retailers are typically notified to accept returns of recalled products and issue refunds, regardless of whether you have a receipt. Check with the store where you purchased the item. Some manufacturers also offer direct refunds — contact the recalling firm using the information in the official recall notice. If you purchased the product online, contact the retailer's customer service with your order number. In either case, you generally do not need original packaging, though retaining the product label with the lot code or UPC can speed up the process.

Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.

The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.

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