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Freshpoint Of Southern Ca Recall: The affected product is being recalled from the marketplace due to possible Salmonella contamination.

United States

TerminatedClass I

Company
Freshpoint Of Southern Ca
Product
Whole cantaloupe 3ct and 6ct brand name Imperial Fresh
Recall date
November 9, 2023
Terminated
July 23, 2024
Source
FDA

Reason for recall

The affected product is being recalled from the marketplace due to possible Salmonella contamination.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Whole cantaloupe 3ct and 6ct brand name Imperial Fresh Not published in this source record 1,802 cases of Imperial Fresh 3ct cantaloupes 198 cases of Imperial Fresh 6ct cantaloupes 10/18/2023 to 11/9/2023

Distribution

  • Food services in California
  • Arizona and Nevada

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0601-2024
Event ID
93427
Status
Terminated
Classification
Class I
Company
Freshpoint Of Southern Ca
Product description
Whole cantaloupe 3ct and 6ct brand name Imperial Fresh
Quantity
1,802 cases of Imperial Fresh 3ct cantaloupes 198 cases of Imperial Fresh 6ct cantaloupes
Reason
The affected product is being recalled from the marketplace due to possible Salmonella contamination.
Recall initiation date
November 9, 2023
Report date
December 13, 2023
Classification date
Not published in this source record
Termination date
July 23, 2024
Distribution pattern
Food services in California, Arizona and Nevada
UPC, lot, and code information
10/18/2023 to 11/9/2023
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Freshpoint Of Southern Ca

Where this information comes from

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

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

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.