Horchata Post Mix Fountain Syrup recall
Recalled by Fiesta Pacific Products Inc. · San Diego, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
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.
Pathogen: Botulism
Clostridium botulinum toxin, a risk in improperly canned or under-processed foods.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Horchata Post Mix Fountain Syrup, 3 gallons (11.4 Liters), UPC 0 09319 00006 0.
Quantity: 13,386 units
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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
Where it was sold
Arizona California Colorado Nevada Utah
FDA's distribution note: CA, NV, UT, CO, AZ
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Fiesta Pacific Products Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 25, 2015
- In FDA report of
- Apr 8, 2015
- Terminated
- Apr 7, 2015
- FDA recall number
- F-1784-2015 · event 70631
- Official record
- FDA enforcement report search