Food Recall Check
Class II · Moderate risk Terminated Initiated Nov 4, 2014 (12 years ago)

Gourmet Warehouse Island Jerk Marinade recall

Recalled by R and S Gourmet Warehouse · Hilton Head Island, SC, United States

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

Why it was recalled

Undeclared non-allergens, soy, wheat, anchovies.

Undeclared allergens: Soy Wheat 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

Gourmet Warehouse, Island Jerk Marinade, 16 fl oz. (473 mL), Ingredient: Soy Sauce, Lemon Juice, Thyme, Allspice, Onion, Garlic, Cayenne Pepper, Salt, Savory Paprika, Spices, P.O. Box 22764, Hilton Head Island, SC 29925.

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.

Expiration date of 08-31-2016 through 11-03-2016

Where it was sold

Alabama Florida Georgia North Carolina South Carolina Tennessee

FDA's distribution note: AL, FL, GA, NC, SC and TN.

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 soy, wheat, 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
R and S Gourmet Warehouse
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 4, 2014
In FDA report of
Dec 10, 2014
Terminated
Mar 5, 2015
FDA recall number
F-0594-2015 · event 69765
Official record
FDA enforcement report search

Also recalled with it (1 more product)

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