Fruit & Vegetable Tray - 64 oz 63912394047 Mixed Melon, Cucumbers & Tajin - 18oz 63912394007 Watermelon & Cucumber
Summary
The FDA issued a Class I for Fruit & Vegetable Tray - 64 oz 63912394047 Mixed Melon, Cucumbers & Tajin - 1 by JFE FRANCHISING INC. Reason: Cucumbers have the potential to be contaminated with Salmonella..
Details
Source
Food Recall
External ID
H-0207-2025
Action Date
2025-07-09
Status
Ongoing
Category
food
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
Lot/Code Info: Sell by 5/20/2025
Quantity Affected: unknown
Reason for Recall
Cucumbers have the potential to be contaminated with Salmonella.
Distribution
AL, IL, IN, KY, MI, TN, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-20
Company
Houston, TX
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 154 food recalls issued in the same week, part of 204 food-related FDA actions this month.
JFE FRANCHISING INC has 20 FDA actions in our database, including 20 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 (JFE FRANCHISING INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does JFE FRANCHISING INC have FDA actions?
JFE FRANCHISING INC has 20 FDA actions in our database, including 20 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0207-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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