Food Recall Check
Class II · Moderate risk Completed Initiated Nov 23, 2022 (4 years ago)

Kerry Pre Idq 61-03 Tnd 50# 227262 300-121584 recall

Recalled by Kerry Inc · Rome, GA, United States

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

Why it was recalled

The firm is recalling their flour based breading due to the presence of egg allergen which is not listed on the label.

Undeclared allergen: Egg

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

KERRY PRE IDQ 61-03 TND 50# 227262 300-121584, NET WEIGHT: 50 LB (22.68KG) INGREDIENTS: Bleached Enriched Wheat Flour***Bread Crumbs***Corn Syrup Solids, Dried Yeast, Soybean Oil, Salt, Mono and Diglycerides, Malted Barley Flour, Ammonium Sulfate, Leavening***Less Than 2% Silicon Dioxide (Anti-Caking), CONTAINS: WHEAT UPC 0 50576 24323 3 Kerry Inc. 3330 MIllington Road, Beloit, WI 53511

Quantity: 24/50 lb bags

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 NUMBER: 0006-458644 BEST BEFORE: 10/14/2023

Where it was sold

Mississippi

FDA's distribution note: Product was shipped to two customers in Mississippi.

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 egg; for anyone else the product is generally not a safety concern. FDA lists this recall as completed: 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
Kerry Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 23, 2022
In FDA report of
Dec 28, 2022
FDA recall number
F-0207-2023 · event 91204
Official record
FDA enforcement report search

Other recalls by Kerry Inc