KERRY PRE IDQ 61-03 TND 50# 227262 300-121584, NET WEIGHT: 50 LB (22.68KG) INGREDIENTS: Bleached Enriched Wheat Flour***
Summary
The FDA issued a Class II for KERRY PRE IDQ 61-03 TND 50# 227262 300-121584, NET WEIGHT: 50 LB (22.68KG) INGRE by Kerry Inc. Reason: The firm is recalling their flour based breading due to the presence of egg allergen which is not listed on the label..
Details
Source
Food Recall
External ID
F-0207-2023
Action Date
2022-12-28
Status
Completed
Category
food
Product Description
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
Lot/Code Info: LOT NUMBER: 0006-458644 BEST BEFORE: 10/14/2023
Quantity Affected: 24/50 lb bags
Reason for Recall
The firm is recalling their flour based breading due to the presence of egg allergen which is not listed on the label.
Distribution
Product was shipped to two customers in Mississippi.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-11-23
Company
Rome, GA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 13 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Kerry Inc has 6 FDA actions in our database, including 6 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Kerry Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kerry Inc have FDA actions?
Kerry Inc has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0207-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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