Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 1, 2011 (15 years ago)

OCHO RIOS***Spicy***Jerk***Curry***Distributed by recall

Recalled by Ocho Rios-Miami, Inc. · Miami, FL, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Whole wheat not declared on label.

Undeclared allergen: Wheat

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

Label reads in part "***OCHO RIOS***Spicy***Jerk***Curry***Distributed by :***Ocho Rios International***Miami, Florida 33142***Ingredients: Turmeric,***Fenugreek, Coriander, Cumin***Salt,*** Anise, Pepper, Pimento, Garlic***Degree of "Heat" 4-Hot***"

Quantity: N/A

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.

Spicy Jerk Curry 4 oz: B/B # K1713 (Exp. 11/17/15) Spicy Jerk Curry 4 oz: B/B # E2015 (Exp. 05/20/15)

Where it was sold

Florida Georgia Illinois Maryland Missouri

FDA's distribution note: FL, GA, IL, MO, MD

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. The risk from an undeclared allergen is to people allergic to wheat; 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
Ocho Rios-Miami, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 1, 2011
In FDA report of
Oct 10, 2012
Terminated
Nov 6, 2014
FDA recall number
F-0004-2013 · event 63018
Official record
FDA enforcement report search

Also recalled with it (3 more products)

FDA files each product of one recall action separately; these share the same FDA event.