RecallHawk
Class I Recall

FreshPoint Bix Produce Company, Cantaloupe. Item # 03143. 3 melons per bag.

Bix Produce Company LLC

Summary

The FDA issued a Class I for FreshPoint Bix Produce Company, Cantaloupe. Item # 03143. 3 melons per bag. by Bix Produce Company LLC. Reason: Cantaloupe may be contaminated with Salmonella..

Details

Source

Food Recall

External ID

F-0304-2024

Action Date

2023-11-08

Status

Terminated

Category

food

Product Description

FreshPoint Bix Produce Company, Cantaloupe. Item # 03143. 3 melons per bag.

Lot/Code Info: Bix Lot Numbers: P2742702-00 and P2741287

Quantity Affected: 61 - 3 packs

Reason for Recall

Cantaloupe may be contaminated with Salmonella.

Distribution

IA, MN, ND, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2023-09-29

Company

Bix Produce Company LLC

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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Bix Produce Company LLC 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 (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 Bix Produce Company LLC have FDA actions?

Bix Produce Company LLC 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-0304-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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