Individually Quick Frozen (IQF) Corn distributed in BULK TOTES (1650lbs and 1750lbs) to consignees for further processin
Summary
The FDA issued a Class II for Individually Quick Frozen (IQF) Corn distributed in BULK TOTES (1650lbs and 1750 by Twin City Foods, Inc.. Reason: Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-1503-2023
Action Date
2023-09-20
Status
Ongoing
Category
food
Product Description
Individually Quick Frozen (IQF) Corn distributed in BULK TOTES (1650lbs and 1750lbs) to consignees for further processing. Bulk tote labels have cooking instructions. Individually Quick Frozen (IQF) Super Sweet Corn, foodservice item, packaged in 32oz. plastic bag, 12 bags per case. The poly bag is stamped with lot code and Product of USA. No UPC. Individually Quick Frozen (IQF) Super Sweet Cut Corn, food service item, packaged in 40oz. poly bags, 12 bags per case. The poly bag is clear (no printing except the coding). Master case label declares KFC Super Sweet Cut Corn, 12-40oz bags, 30lbs. UPC 885251248124.
Lot/Code Info: Bulk Totes: Shop Orders 21369 and 21373. Manufactured on 8/21/2022. Corn 32oz: 83012. KFC Corn 40oz: Use by Oct 24 2024 82972 554922 822315.
Quantity Affected: Bulk Totes Total: 66,300 lbs; Corn: 610 cases (12/32oz. bags per case) and 635 cases (12/40oz. bags per case)
Reason for Recall
Listeria monocytogenes
Distribution
distributed nationwide in the US and in Costa Rica, China, and Japan.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-18
Company
Stanwood, WA
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 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Twin City Foods, Inc. has 4 FDA actions in our database, including 4 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 (Twin City Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Twin City Foods, Inc. have FDA actions?
Twin City Foods, Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1503-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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