Fruit Medley Cup 16/6 oz 3300-3 Cantaloupe Cube (2/5 lb) 3338-3 Fruit Mix Kit (4/5 lb) (Tray) 2963-3 3 Melon 16/6 oz cup
Summary
The FDA issued a Class I for Fruit Medley Cup 16/6 oz 3300-3 Cantaloupe Cube (2/5 lb) 3338-3 Fruit Mix Kit (4 by Vinyard Fruit & Vegetable Co., LLC. Reason: The affected product is being recalled from the marketplace due to possible Salmonella contamination..
Details
Source
Food Recall
External ID
F-0578-2024
Action Date
2023-12-20
Status
Terminated
Category
food
Product Description
Fruit Medley Cup 16/6 oz 3300-3 Cantaloupe Cube (2/5 lb) 3338-3 Fruit Mix Kit (4/5 lb) (Tray) 2963-3 3 Melon 16/6 oz cups 3330-3 Fruit Mix (2/5 lb) 3301-3 Cantaloupe Cube (5 lb) 3304-3 Cantaloupe Cubed 10/12 oz cups 0526-3 Melon Variety Pack 2964-3 3 Melon Medley 6 oz cups 2973-3 Fruit Medley 6 oz cups 2976-3 Cantaloupe Chunks 6 oz cups
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Quantity Affected: 599 cases and 459 each
Reason for Recall
The affected product is being recalled from the marketplace due to possible Salmonella contamination.
Distribution
Product was all distributed within the state of Oklahoma. Product was distributed to food services, distributions centers and to 7-11 convenience stores.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-10
Company
Oklahoma City, OK
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 143 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 (Vinyard Fruit & Vegetable Co., LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Vinyard Fruit & Vegetable Co., LLC have FDA actions?
This is the only FDA action we have on record for Vinyard Fruit & Vegetable Co., LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0578-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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