Cantaloupe Fruit Cup, Item 19703. clam-shell container. Net Wt 5.75 oz (163g). UPC 8 46709-00523 2. Manufactured a
Summary
The FDA issued a Class I for Cantaloupe Fruit Cup, Item 19703. clam-shell container. Net Wt 5.75 oz (163g by FreshPoint Bix Produce Company, LLC. Reason: Potential Salmonella contamination..
Details
Source
Food Recall
External ID
F-0666-2024
Action Date
2023-12-13
Status
Terminated
Category
food
Product Description
Cantaloupe Fruit Cup, Item 19703. clam-shell container. Net Wt 5.75 oz (163g). UPC 8 46709-00523 2. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117
Lot/Code Info: Lot number / Sales Order #: 05959648 and 05960814 Sell By 10/25/2023 and 10/26/2023.
Quantity Affected: 10 units
Reason for Recall
Potential Salmonella contamination.
Distribution
IA, MN, ND, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-17
Company
Little Canada, MN
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 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
FreshPoint Bix Produce Company, LLC has 8 FDA actions in our database, including 8 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 (FreshPoint Bix Produce Company, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does FreshPoint Bix Produce Company, LLC have FDA actions?
FreshPoint Bix Produce Company, LLC has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0666-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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