Private Selection 48oz Classic Fruit Medley, frozen product, 8/48 oz bags per case. UPC 0 11110 82026 6. Distributed by
Summary
The FDA issued a Class I for Private Selection 48oz Classic Fruit Medley, frozen product, 8/48 oz bags per ca by Townsend Farms Inc. Reason: Potential to be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-1272-2023
Action Date
2023-07-26
Status
Terminated
Category
food
Product Description
Private Selection 48oz Classic Fruit Medley, frozen product, 8/48 oz bags per case. UPC 0 11110 82026 6. Distributed by The Kroger Co. Cincinnati, OH
Lot/Code Info: BEST IF USED BY: 05/03/24 05/04/24 05/10/24 05/18/24 CODES: 05/03/24 T3 PRODUCT OF USA, MEXICO, CHILE & COSTA RICA F2202220 05/03/24 T3 PRODUCT OF USA, MEXICO, CHILE & COSTARICA F2202213 05/04/24 T3 PRODUCT OF USA, MEXICO, CHILE & COSTA RICA F2202226 05/04/24 T3 PRODUCT OF USA, MEXICO, CHILE & COSTA RICA F2202230 05/10/24 T3 PRODUCT OF USA, MEXICO, PERU, CHILE & COSTA RICA F2202268 05/10/24 T3 PRODUCT OF USA, MEXICO, PERU, CHILE & COSTA RICA F2202273 05/18/24 T3 PRODUCT OF USA, MEXICO, CHILE, PERU & COSTA RICA F2202319 05/18/24 T3 PRODUCT OF USA, MEXICO, CHILE, PERU & COSTARICA F2202325
Quantity Affected: 86,200 bags (48 oz. per bag)
Reason for Recall
Potential to be contaminated with Listeria monocytogenes.
Distribution
Distributed in Alabama, Arkansas, Georgia, Illinois, Indiana, Kentucky, Louisiana, Michigan, Missouri, Mississippi, Ohio, South Carolina, Tennessee, Texas, Virginia, and West Virginia.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-06-21
Company
Fairview, OR
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 61 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Townsend Farms Inc has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Townsend Farms Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Townsend Farms Inc have FDA actions?
Townsend Farms 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-1272-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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