Seasonal Blend 10oz, Seasonal Blend 16oz, Seasonal Blend 42oz , Melon Trio 16oz, Melon Mix 32oz, Fruit Blend 16oz, Fruit
Summary
The FDA issued a Class I for Seasonal Blend 10oz, Seasonal Blend 16oz, Seasonal Blend 42oz , Melon Trio 16oz, by CF Dallas LLC. Reason: The select fresh-cut products were made from whole cantaloupe subject to a previously announced voluntary recall initiated by Sofia Produce, LLC dba T.
Details
Source
Food Recall
External ID
F-0772-2024
Action Date
2024-01-24
Status
Terminated
Category
food
Product Description
Seasonal Blend 10oz, Seasonal Blend 16oz, Seasonal Blend 42oz , Melon Trio 16oz, Melon Mix 32oz, Fruit Blend 16oz, Fruit Bowl 40oz, Seasonal Fruit Tray 48oz, Fruit Mix 32oz, Cantaloupe Chunks 10oz, Cantaloupe Chunks 16oz, Fruit Medley 6oz- all packaged in clear plastic clamshells/ cups
Lot/Code Info: NCC 0103 NCN 0103
Quantity Affected: 27,998 units
Reason for Recall
The select fresh-cut products were made from whole cantaloupe subject to a previously announced voluntary recall initiated by Sofia Produce, LLC dba Trufresh. The whole cantaloupe may have the potential to be contaminated with Salmonella.
Distribution
Select retail stores in Indiana, Michigan, Ohio, Kentucky, North Carolina, Tennessee, Virginia, Illinois, Texas, and Louisiana
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-20
Company
Grand Prairie, TX
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 81 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (CF Dallas LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does CF Dallas LLC have FDA actions?
This is the only FDA action we have on record for CF Dallas LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0772-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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