Pico De Gallo
Reason Potential contamination with Salmonella.
Dip Trio Mix Homemade Gourmet Dip Mix recall
Recalled by Phoenix Food, LLC · Canton, TX, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Possible Salmonella contamination.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
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
Dip Trio Mix Homemade Gourmet Dip Mix Net Wt. 2.9 oz. Distributed by: Phoenix Food, LLC. Canton, TX 75103 www.homemadegourmet.com
Quantity: 11,936 boxes
Food: Sauces, dips & dressings
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.
Lot: K110420161, K111220161, K111120161
Where it was sold
Alabama Arkansas California Colorado Georgia Iowa Illinois Indiana Kansas Massachusetts Michigan Minnesota Missouri Mississippi New York Ohio Pennsylvania South Carolina South Dakota Tennessee Texas Virginia Washington Wisconsin
FDA's distribution note: CO, WA, TX, SC, PA, NY, WI, VA, CA, MO, KS, IN, AR, AL, SD, OH, Canada, GA, MA, MN, TN, IA, MI, MS, IL
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- Phoenix Food, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 26, 2017
- In FDA report of
- May 31, 2017
- Terminated
- Mar 27, 2018
- FDA recall number
- F-2245-2017 · event 77142
- Official record
- FDA enforcement report search
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