Food Recall Check
Class I · High risk Terminated Initiated Jan 2, 2022 (5 years ago)

CHICKEN SALAD Croissant recall

Recalled by Renaissance Food Group, LLC · Rancho Cordova, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

The firm discovered that some of their Chicken Salad Croissants contained Tuna Salad. Fish is not declared on the label.

Undeclared allergen: 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

CHICKEN SALAD Croissant NET WT. 7.8OZ (221g) Perishable, Keep Refrigerated Ingredients: Chicken Salad***Savory Mayonnaise Base***Croissant***Lettuce. CONTIANS EGG, MILK, WHEAT, SOY, MAY CONTAIN TREE NUTS. Dist. By: Renaissance Food Group, LLC 4322 Moreland Ave. Conley, GA 30288 UPC 8 26766 15578 1

Quantity: 266/7.8oz packages

Food: Salads, sandwiches & prepared foods

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.

Sell By: 01/04/22 GHGA 364

Where it was sold

Alabama Georgia South Carolina

FDA's distribution note: Product was shipped to AL, GA & SC

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 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
Renaissance Food Group, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 2, 2022
In FDA report of
Jan 19, 2022
Terminated
Feb 10, 2022
FDA recall number
F-0383-2022 · event 89332
Official record
FDA enforcement report search

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