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Bix Produce Company LLC Recall: Cantaloupe may be contaminated with Salmonella.

United States

TerminatedClass I

Company
Bix Produce Company LLC
Product
FreshPoint Bix Produce Company, Cantaloupe. Item # 03143.…
Recall date
September 29, 2023
Terminated
January 11, 2024
Source
FDA

Reason for recall

Cantaloupe may be contaminated with Salmonella.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
FreshPoint Bix Produce Company, Cantaloupe. Item # 03143. 3 melons per bag. Not published in this source record 61 - 3 packs Bix Lot Numbers: P2742702-00 and P2741287

Distribution

  • IA
  • MN
  • ND
  • WI

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0304-2024
Event ID
93162
Status
Terminated
Classification
Class I
Company
Bix Produce Company LLC
Product description
FreshPoint Bix Produce Company, Cantaloupe. Item # 03143. 3 melons per bag.
Quantity
61 - 3 packs
Reason
Cantaloupe may be contaminated with Salmonella.
Recall initiation date
September 29, 2023
Report date
November 8, 2023
Classification date
Not published in this source record
Termination date
January 11, 2024
Distribution pattern
IA, MN, ND, WI
UPC, lot, and code information
Bix Lot Numbers: P2742702-00 and P2741287
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Bix Produce Company LLC

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Distribution
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Product
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Published
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Distribution
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Product
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Published
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Distribution
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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Iowa 1
Minnesota 1
North Dakota 1
Wisconsin 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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