Cucumber Diced Greek Cut (1/8"x1/8"x1"), 360# Drum with poly liner item C0376, 30# Box with poly liner item C0369. Cucum
Summary
The FDA issued a Class I for Cucumber Diced Greek Cut (1/8"x1/8"x1"), 360# Drum with poly liner item C0376, 3 by E-Z SPUDS INC. Reason: Potential for Salmonella.
Details
Source
Food Recall
External ID
F-0315-2025
Action Date
2025-01-01
Status
Terminated
Category
food
Product Description
Cucumber Diced Greek Cut (1/8"x1/8"x1"), 360# Drum with poly liner item C0376, 30# Box with poly liner item C0369. Cucumber Diced Regular Cut (1/8"x1/8"x1/4"), 300# Drum with poly liner item C0390, 30# Box with poly line C0383
Lot/Code Info: Cucumber Diced Greek Cut (1/8"x1/8"x1") Dates of Mfg - 10/28/2024, 10/29/2024, 10/31/2024 Cucumber Diced Regular Cut (1/8"x1/8"x1/4") Dates of Mfg - 10/25/2024, 10/30/2024
Quantity Affected: 23,340 lbs.
Reason for Recall
Potential for Salmonella
Distribution
IL
Type: Voluntary: Firm initiated
Recall Initiated: 2024-11-29
Company
Melrose Park, IL
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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
E-Z SPUDS INC has 11 FDA actions in our database, including 11 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 (E-Z SPUDS INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does E-Z SPUDS INC have FDA actions?
E-Z SPUDS INC has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0315-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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