Pico De Gallo
Reason Potential contamination with Salmonella.
Floribbean Key Lime Calypso Dip recall
Recalled by Miami Interculinary Center, Inc. · Miami, FL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
During an FDA inspection a product was found that the label fail to declared the component ingredients of all its compound ingredients like Mayonnaise and Worcestershire sauce that contains allergens like eggs, soy, and anchovies.
Undeclared allergens: Egg Soy Fish
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Floribbean Key Lime Calypso Dip 12.5 oz Floribbean 68 SW 40 St. Suite 411 Miami, Florida 33155 1(800)282-8459
Quantity: 1,164 bottles
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 # 07171311
Where it was sold
California Florida Georgia Illinois Maryland North Carolina Ohio Pennsylvania Virginia Washington
FDA's distribution note: CA, FL, GA, IL, MD, NC, OH, PA, VA, and WA
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. The risk from an undeclared allergen is to people allergic to egg, soy, fish; for anyone else the product is generally not a safety concern. 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
- Miami Interculinary Center, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 23, 2014
- In FDA report of
- Jul 2, 2014
- Terminated
- Aug 2, 2019
- FDA recall number
- F-2030-2014 · event 68005
- Official record
- FDA enforcement report search
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