E-z Spuds Inc food recall: Cucumber Diced Greek Cut
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 95923
- Recall initiated
- Nov 29, 2024
- Classified by FDA
- Dec 20, 2024
- Posted in Enforcement Report
- Jan 1, 2025
- Terminated
- Jan 31, 2025
- Recalling firm
- E-Z SPUDS INC
- Firm location
- Melrose Park, IL, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Potential for Salmonella
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Nov 29, 2024. FDA classified it 21 days later, on Dec 20, 2024. Distribution reported by FDA: IL E-Z SPUDS INC has 2 recalls in our records.
Recalled products (1)
F-0315-2025 Class I Terminated
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
Codes / lots: 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: 23,340 lbs.
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 95923
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.