RecallHawk
Class I Recall

Cucumber with Ranch - 9 oz 63912395020 Cucumber, Lime & Tajin - 19oz 63912388053 Cucumber Slices w/Tajin - 15 oz

JFE FRANCHISING INC

Summary

The FDA issued a Class I for Cucumber with Ranch - 9 oz 63912395020 Cucumber, Lime & Tajin - 19oz 63912 by JFE FRANCHISING INC. Reason: Cucumbers have the potential to be contaminated with Salmonella..

Details

Source

Food Recall

External ID

H-0206-2025

Action Date

2025-07-09

Status

Ongoing

Category

food

Product Description

Cucumber with Ranch - 9 oz 63912395020 Cucumber, Lime & Tajin - 19oz 63912388053 Cucumber Slices w/Tajin - 15 oz 63912388022 Cucumber Bowl w/ Ranch Dressing - 15 oz 63912388063

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

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-0206-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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