JFE FRANCHISING INC Recall: Cucumbers have the potential to be contaminated with Salmonella.

🇺🇸 United States

1. May 20, 2025 - Recall initiated
2. July 9, 2025 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0207-2025

Event ID

96933

Status

Ongoing

Classification

Class I

Company

JFE FRANCHISING INC

Product description

Fruit & Vegetable Tray - 64 oz 63912394047 Mixed Melon, Cucumbers & Tajin - 18oz 63912394007 Watermelon & Cucumber w/ Tajin - 18oz 63912394036 Small Vegetable Tray - 19.5 oz 63912388045 Small Party Tray with Dip - 19 oz 63912388046 Large Vegetable Tray - 42 oz 63912388056 Vegetable Bowl - 26 oz 63912388044 Vegetable Bowl - 13 oz 63912388072 Baby Carrot, Cucumber, & Ranch - 15 oz 63912394045 Signature Vegetable Bowl - 28 oz 639123600172

Quantity

unknown

Reason

Cucumbers have the potential to be contaminated with Salmonella.

Recall initiation date

May 20, 2025

Report date

July 9, 2025

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

AL, IL, IN, KY, MI, TN, WI

UPC, lot, and code information

Sell by 5/20/2025

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 96933 with 4 other product entries in Public Health Trace.

Responsible company: JFE FRANCHISING INC

Other recalls from JFE FRANCHISING INC

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

Distributed No data published

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
Alabama	1
Illinois	1
Indiana	1
Kentucky	1
Michigan	1
Tennessee	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: July 18, 2026 ET

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 "Ongoing." 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.

• Email
• X / Twitter
• Facebook